Name: rs9614
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs9614

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:11650504 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: T>A / T>G
Variation Type: SNV Single Nucleotide Variation
Frequency: G=0.204205 (54051/264690, TOPMED)
G=0.197999 (49666/250840, ALFA)
G=0.221083 (51458/232754, GnomAD_exome) (+ 23 more)
G=0.194793 (27310/140200, GnomAD)
G=0.26117 (22875/87586, ExAC)
G=0.44245 (12501/28254, 14KJPN)
G=0.44069 (7385/16758, 8.3KJPN)
G=0.18339 (2383/12994, GO-ESP)
G=0.2380 (1524/6404, 1000G_30x)
G=0.2436 (1220/5008, 1000G)
G=0.1743 (781/4480, Estonian)
G=0.1866 (719/3854, ALSPAC)
G=0.1888 (700/3708, TWINSUK)
G=0.4689 (1373/2928, KOREAN)
G=0.2800 (583/2082, HGDP_Stanford)
G=0.2341 (443/1892, HapMap)
G=0.4436 (810/1826, Korea1K)
G=0.443 (272/614, Vietnamese)
G=0.182 (109/600, NorthernSweden)
G=0.036 (19/534, MGP)
T=0.403 (112/278, SGDP_PRJ)
G=0.170 (45/264, FINRISK)
G=0.130 (28/216, Qatari)
G=0.15 (8/52, Ancient Sardinia)
G=0.15 (6/40, GENOME_DK)
T=0.42 (11/26, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: FBXO2 : Missense Variant
Publications: 1 citation
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20230706150541

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	266802	T=0.803097	G=0.196903
European	Sub	225670	T=0.804600	G=0.195400
African	Sub	12304	T=0.82884	G=0.17116
African Others	Sub	452	T=0.847	G=0.153
African American	Sub	11852	T=0.82813	G=0.17187
Asian	Sub	802	T=0.537	G=0.463
East Asian	Sub	626	T=0.534	G=0.466
Other Asian	Sub	176	T=0.551	G=0.449
Latin American 1	Sub	1194	T=0.7973	G=0.2027
Latin American 2	Sub	6916	T=0.7636	G=0.2364
South Asian	Sub	5042	T=0.7836	G=0.2164
Other	Sub	14874	T=0.79878	G=0.20122

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	T=0.795795	G=0.204205
Allele Frequency Aggregator	Total	Global	250840	T=0.802001	G=0.197999
Allele Frequency Aggregator	European	Sub	215914	T=0.804098	G=0.195902
Allele Frequency Aggregator	Other	Sub	13456	T=0.79838	G=0.20162
Allele Frequency Aggregator	African	Sub	7516	T=0.8249	G=0.1751
Allele Frequency Aggregator	Latin American 2	Sub	6916	T=0.7636	G=0.2364
Allele Frequency Aggregator	South Asian	Sub	5042	T=0.7836	G=0.2164
Allele Frequency Aggregator	Latin American 1	Sub	1194	T=0.7973	G=0.2027
Allele Frequency Aggregator	Asian	Sub	802	T=0.537	G=0.463
gnomAD - Exomes	Global	Study-wide	232754	T=0.778917	G=0.221083
gnomAD - Exomes	European	Sub	124130	T=0.805180	G=0.194820
gnomAD - Exomes	Asian	Sub	46010	T=0.68539	G=0.31461
gnomAD - Exomes	American	Sub	33042	T=0.76651	G=0.23349
gnomAD - Exomes	African	Sub	14256	T=0.83361	G=0.16639
gnomAD - Exomes	Ashkenazi Jewish	Sub	9614	T=0.8380	G=0.1620
gnomAD - Exomes	Other	Sub	5702	T=0.7973	G=0.2027
gnomAD - Genomes	Global	Study-wide	140200	T=0.805207	G=0.194793
gnomAD - Genomes	European	Sub	75916	T=0.80568	G=0.19432
gnomAD - Genomes	African	Sub	42030	T=0.83267	G=0.16733
gnomAD - Genomes	American	Sub	13654	T=0.77230	G=0.22770
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	T=0.8421	G=0.1579
gnomAD - Genomes	East Asian	Sub	3124	T=0.5317	G=0.4683
gnomAD - Genomes	Other	Sub	2152	T=0.8011	G=0.1989
ExAC	Global	Study-wide	87586	T=0.73883	G=0.26117
ExAC	Europe	Sub	51802	T=0.76387	G=0.23613
ExAC	Asian	Sub	20334	T=0.66268	G=0.33732
ExAC	American	Sub	7926	T=0.7180	G=0.2820
ExAC	African	Sub	6916	T=0.7976	G=0.2024
ExAC	Other	Sub	608	T=0.755	G=0.245
14KJPN	JAPANESE	Study-wide	28254	T=0.55755	G=0.44245
8.3KJPN	JAPANESE	Study-wide	16758	T=0.55931	G=0.44069
GO Exome Sequencing Project	Global	Study-wide	12994	T=0.81661	G=0.18339
GO Exome Sequencing Project	European American	Sub	8596	T=0.8077	G=0.1923
GO Exome Sequencing Project	African American	Sub	4398	T=0.8340	G=0.1660
1000Genomes_30x	Global	Study-wide	6404	T=0.7620	G=0.2380
1000Genomes_30x	African	Sub	1786	T=0.8494	G=0.1506
1000Genomes_30x	Europe	Sub	1266	T=0.8318	G=0.1682
1000Genomes_30x	South Asian	Sub	1202	T=0.7729	G=0.2271
1000Genomes_30x	East Asian	Sub	1170	T=0.5556	G=0.4444
1000Genomes_30x	American	Sub	980	T=0.746	G=0.254
1000Genomes	Global	Study-wide	5008	T=0.7564	G=0.2436
1000Genomes	African	Sub	1322	T=0.8570	G=0.1430
1000Genomes	East Asian	Sub	1008	T=0.5506	G=0.4494
1000Genomes	Europe	Sub	1006	T=0.8241	G=0.1759
1000Genomes	South Asian	Sub	978	T=0.772	G=0.228
1000Genomes	American	Sub	694	T=0.744	G=0.256
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.8257	G=0.1743
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.8134	G=0.1866
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.8112	G=0.1888
KOREAN population from KRGDB	KOREAN	Study-wide	2928	T=0.5311	A=0.0000, G=0.4689
HGDP-CEPH-db Supplement 1	Global	Study-wide	2082	T=0.7200	G=0.2800
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	T=0.577	G=0.423
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	T=0.746	G=0.254
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	T=0.797	G=0.203
HGDP-CEPH-db Supplement 1	Europe	Sub	320	T=0.769	G=0.231
HGDP-CEPH-db Supplement 1	Africa	Sub	242	T=0.822	G=0.178
HGDP-CEPH-db Supplement 1	America	Sub	216	T=0.662	G=0.338
HGDP-CEPH-db Supplement 1	Oceania	Sub	70	T=0.74	G=0.26
HapMap	Global	Study-wide	1892	T=0.7659	G=0.2341
HapMap	American	Sub	770	T=0.739	G=0.261
HapMap	African	Sub	692	T=0.868	G=0.132
HapMap	Asian	Sub	254	T=0.535	G=0.465
HapMap	Europe	Sub	176	T=0.812	G=0.188
Korean Genome Project	KOREAN	Study-wide	1826	T=0.5564	G=0.4436
A Vietnamese Genetic Variation Database	Global	Study-wide	614	T=0.557	G=0.443
Northern Sweden	ACPOP	Study-wide	600	T=0.818	G=0.182
Medical Genome Project healthy controls from Spanish population	Spanish controls	Study-wide	534	T=0.964	G=0.036
SGDP_PRJ	Global	Study-wide	278	T=0.403	G=0.597
FINRISK	Finnish from FINRISK project	Study-wide	264	T=0.830	G=0.170
Qatari	Global	Study-wide	216	T=0.870	G=0.130
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	52	T=0.85	G=0.15
The Danish reference pan genome	Danish	Study-wide	40	T=0.85	G=0.15
Siberian	Global	Study-wide	26	T=0.42	G=0.58

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 1	NC_000001.11:g.11650504T>A
GRCh38.p14 chr 1	NC_000001.11:g.11650504T>G
GRCh37.p13 chr 1	NC_000001.10:g.11710561T>A
GRCh37.p13 chr 1	NC_000001.10:g.11710561T>G

Gene: FBXO2, F-box protein 2 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
FBXO2 transcript	NM_012168.6:c.353A>T	K [AAG] > M [ATG]	Coding Sequence Variant
F-box only protein 2	NP_036300.2:p.Lys118Met	K (Lys) > M (Met)	Missense Variant
FBXO2 transcript	NM_012168.6:c.353A>C	K [AAG] > T [ACG]	Coding Sequence Variant
F-box only protein 2	NP_036300.2:p.Lys118Thr	K (Lys) > T (Thr)	Missense Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	T=	A	G
GRCh38.p14 chr 1	NC_000001.11:g.11650504=	NC_000001.11:g.11650504T>A	NC_000001.11:g.11650504T>G
GRCh37.p13 chr 1	NC_000001.10:g.11710561=	NC_000001.10:g.11710561T>A	NC_000001.10:g.11710561T>G
FBXO2 transcript	NM_012168.6:c.353=	NM_012168.6:c.353A>T	NM_012168.6:c.353A>C
FBXO2 transcript	NM_012168.5:c.353=	NM_012168.5:c.353A>T	NM_012168.5:c.353A>C
F-box only protein 2	NP_036300.2:p.Lys118=	NP_036300.2:p.Lys118Met	NP_036300.2:p.Lys118Thr

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

139 SubSNP, 26 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	CGAP-GAI	ss11719	Sep 19, 2000 (52)
2	TSC-CSHL	ss1343940	Oct 04, 2000 (86)
3	LEE	ss4397096	May 29, 2002 (106)
4	SEQUENOM	ss24780393	Sep 20, 2004 (126)
5	SEQUENOM	ss24790484	Sep 20, 2004 (126)
6	ILLUMINA	ss65732162	Oct 13, 2006 (127)
7	ILLUMINA	ss66695693	Nov 29, 2006 (127)
8	ILLUMINA	ss67936581	Nov 29, 2006 (127)
9	ILLUMINA	ss68054341	Nov 29, 2006 (127)
10	ILLUMINA	ss71619073	May 16, 2007 (127)
11	ILLUMINA	ss75589698	Dec 07, 2007 (129)
12	ILLUMINA	ss79301462	Dec 15, 2007 (130)
13	KRIBB_YJKIM	ss83349217	Dec 15, 2007 (130)
14	CANCER-GENOME	ss86341819	Mar 23, 2008 (129)
15	ILLUMINA	ss98278251	May 26, 2008 (130)
16	ILLUMINA-UK	ss118499144	Feb 14, 2009 (130)
17	ILLUMINA	ss123022319	Dec 01, 2009 (131)
18	ILLUMINA	ss154504086	Dec 01, 2009 (131)
19	GMI	ss154639515	Dec 01, 2009 (131)
20	ILLUMINA	ss159677965	Dec 01, 2009 (131)
21	SEATTLESEQ	ss159696078	Dec 01, 2009 (131)
22	ILLUMINA	ss161003807	Dec 01, 2009 (131)
23	ILLUMINA	ss172487149	Jul 04, 2010 (132)
24	ILLUMINA	ss174877960	Jul 04, 2010 (132)
25	BUSHMAN	ss198022865	Jul 04, 2010 (132)
26	1000GENOMES	ss217314416	Jul 14, 2010 (132)
27	1000GENOMES	ss217390856	Jul 14, 2010 (132)
28	1000GENOMES	ss217392087	Jul 14, 2010 (132)
29	1000GENOMES	ss217399977	Jul 14, 2010 (132)
30	1000GENOMES	ss217405871	Jul 14, 2010 (132)
31	1000GENOMES	ss217410518	Jul 14, 2010 (132)
32	1000GENOMES	ss217410996	Jul 14, 2010 (132)
33	1000GENOMES	ss218237779	Jul 14, 2010 (132)
34	1000GENOMES	ss230427141	Jul 14, 2010 (132)
35	1000GENOMES	ss238142409	Jul 15, 2010 (132)
36	GMI	ss275714798	May 04, 2012 (137)
37	NHLBI-ESP	ss341932891	May 09, 2011 (134)
38	ILLUMINA	ss481950922	May 04, 2012 (137)
39	ILLUMINA	ss481984517	May 04, 2012 (137)
40	ILLUMINA	ss482939593	Sep 08, 2015 (146)
41	ILLUMINA	ss485769124	May 04, 2012 (137)
42	1000GENOMES	ss489720754	May 04, 2012 (137)
43	EXOME_CHIP	ss491286197	May 04, 2012 (137)
44	CLINSEQ_SNP	ss491584486	May 04, 2012 (137)
45	ILLUMINA	ss537617591	Sep 08, 2015 (146)
46	TISHKOFF	ss553800307	Apr 25, 2013 (138)
47	SSMP	ss647576793	Apr 25, 2013 (138)
48	ILLUMINA	ss778644452	Sep 08, 2015 (146)
49	ILLUMINA	ss783330387	Sep 08, 2015 (146)
50	ILLUMINA	ss784282108	Sep 08, 2015 (146)
51	ILLUMINA	ss825631980	Apr 01, 2015 (144)
52	ILLUMINA	ss832592155	Sep 08, 2015 (146)
53	ILLUMINA	ss833188672	Jul 12, 2019 (153)
54	ILLUMINA	ss834102186	Sep 08, 2015 (146)
55	JMKIDD_LAB	ss974433201	Aug 21, 2014 (142)
56	EVA-GONL	ss974858980	Aug 21, 2014 (142)
57	JMKIDD_LAB	ss1067416122	Aug 21, 2014 (142)
58	JMKIDD_LAB	ss1067671660	Aug 21, 2014 (142)
59	1000GENOMES	ss1289696571	Aug 21, 2014 (142)
60	EVA_GENOME_DK	ss1573888548	Apr 01, 2015 (144)
61	EVA_FINRISK	ss1584004640	Apr 01, 2015 (144)
62	EVA_DECODE	ss1584217171	Apr 01, 2015 (144)
63	EVA_UK10K_ALSPAC	ss1599555197	Apr 01, 2015 (144)
64	EVA_UK10K_TWINSUK	ss1642549230	Apr 01, 2015 (144)
65	EVA_EXAC	ss1685301788	Apr 01, 2015 (144)
66	EVA_MGP	ss1710888147	Apr 01, 2015 (144)
67	EVA_SVP	ss1712311346	Apr 01, 2015 (144)
68	ILLUMINA	ss1751865786	Sep 08, 2015 (146)
69	HAMMER_LAB	ss1793909905	Sep 08, 2015 (146)
70	WEILL_CORNELL_DGM	ss1918058755	Feb 12, 2016 (147)
71	JJLAB	ss2019543203	Sep 14, 2016 (149)
72	USC_VALOUEV	ss2147541119	Dec 20, 2016 (150)
73	HUMAN_LONGEVITY	ss2160077029	Dec 20, 2016 (150)
74	SYSTEMSBIOZJU	ss2624287967	Nov 08, 2017 (151)
75	ILLUMINA	ss2632477777	Nov 08, 2017 (151)
76	GRF	ss2697437711	Nov 08, 2017 (151)
77	ILLUMINA	ss2710665674	Nov 08, 2017 (151)
78	GNOMAD	ss2731117153	Nov 08, 2017 (151)
79	GNOMAD	ss2746214301	Nov 08, 2017 (151)
80	GNOMAD	ss2751661248	Nov 08, 2017 (151)
81	AFFY	ss2984845249	Nov 08, 2017 (151)
82	SWEGEN	ss2986301573	Nov 08, 2017 (151)
83	BIOINF_KMB_FNS_UNIBA	ss3023535795	Nov 08, 2017 (151)
84	CSHL	ss3343318938	Nov 08, 2017 (151)
85	ILLUMINA	ss3626026720	Oct 11, 2018 (152)
86	ILLUMINA	ss3630516181	Oct 11, 2018 (152)
87	ILLUMINA	ss3632880852	Oct 11, 2018 (152)
88	ILLUMINA	ss3633574679	Oct 11, 2018 (152)
89	ILLUMINA	ss3634306931	Oct 11, 2018 (152)
90	ILLUMINA	ss3635268803	Oct 11, 2018 (152)
91	ILLUMINA	ss3635983063	Oct 11, 2018 (152)
92	ILLUMINA	ss3637019170	Oct 11, 2018 (152)
93	ILLUMINA	ss3637737437	Oct 11, 2018 (152)
94	ILLUMINA	ss3638890000	Oct 11, 2018 (152)
95	ILLUMINA	ss3639441870	Oct 11, 2018 (152)
96	ILLUMINA	ss3640014295	Oct 11, 2018 (152)
97	ILLUMINA	ss3642751304	Oct 11, 2018 (152)
98	OMUKHERJEE_ADBS	ss3646221271	Oct 11, 2018 (152)
99	ILLUMINA	ss3653618881	Oct 11, 2018 (152)
100	EGCUT_WGS	ss3654402323	Jul 12, 2019 (153)
101	EVA_DECODE	ss3686170331	Jul 12, 2019 (153)
102	ACPOP	ss3726793113	Jul 12, 2019 (153)
103	ILLUMINA	ss3744607913	Jul 12, 2019 (153)
104	EVA	ss3745833591	Jul 12, 2019 (153)
105	ILLUMINA	ss3772109525	Jul 12, 2019 (153)
106	KHV_HUMAN_GENOMES	ss3798853849	Jul 12, 2019 (153)
107	EVA	ss3823559797	Apr 25, 2020 (154)
108	EVA	ss3825553341	Apr 25, 2020 (154)
109	EVA	ss3826024974	Apr 25, 2020 (154)
110	HGDP	ss3847324577	Apr 25, 2020 (154)
111	SGDP_PRJ	ss3848200680	Apr 25, 2020 (154)
112	KRGDB	ss3893085775	Apr 25, 2020 (154)
113	KOGIC	ss3943832062	Apr 25, 2020 (154)
114	FSA-LAB	ss3983915807	Apr 25, 2021 (155)
115	FSA-LAB	ss3983915808	Apr 25, 2021 (155)
116	EVA	ss3984778697	Apr 25, 2021 (155)
117	EVA	ss3986008466	Apr 25, 2021 (155)
118	EVA	ss3986098831	Apr 25, 2021 (155)
119	EVA	ss4016893418	Apr 25, 2021 (155)
120	TOPMED	ss4439338763	Apr 25, 2021 (155)
121	TOMMO_GENOMICS	ss5142492457	Apr 25, 2021 (155)
122	EVA	ss5236864153	Apr 25, 2021 (155)
123	1000G_HIGH_COVERAGE	ss5241189044	Oct 12, 2022 (156)
124	EVA	ss5314593150	Oct 12, 2022 (156)
125	EVA	ss5316773859	Oct 12, 2022 (156)
126	HUGCELL_USP	ss5442391673	Oct 12, 2022 (156)
127	1000G_HIGH_COVERAGE	ss5512953089	Oct 12, 2022 (156)
128	EVA	ss5623987353	Oct 12, 2022 (156)
129	SANFORD_IMAGENETICS	ss5624932091	Oct 12, 2022 (156)
130	TOMMO_GENOMICS	ss5666800304	Oct 12, 2022 (156)
131	EVA	ss5799407201	Oct 12, 2022 (156)
132	EVA	ss5799475119	Oct 12, 2022 (156)
133	EVA	ss5800077774	Oct 12, 2022 (156)
134	YY_MCH	ss5800326038	Oct 12, 2022 (156)
135	EVA	ss5831544693	Oct 12, 2022 (156)
136	EVA	ss5848247877	Oct 12, 2022 (156)
137	EVA	ss5848784965	Oct 12, 2022 (156)
138	EVA	ss5907058261	Oct 12, 2022 (156)
139	EVA	ss5936759062	Oct 12, 2022 (156)
140	1000Genomes	NC_000001.10 - 11710561	Oct 11, 2018 (152)
141	1000Genomes_30x	NC_000001.11 - 11650504	Oct 12, 2022 (156)
142	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 11710561	Oct 11, 2018 (152)
143	Genetic variation in the Estonian population	NC_000001.10 - 11710561	Oct 11, 2018 (152)
144	ExAC	NC_000001.10 - 11710561	Oct 11, 2018 (152)
145	FINRISK	NC_000001.10 - 11710561	Apr 25, 2020 (154)
146	The Danish reference pan genome	NC_000001.10 - 11710561	Apr 25, 2020 (154)
147	gnomAD - Genomes	NC_000001.11 - 11650504	Apr 25, 2021 (155)
148	gnomAD - Exomes	NC_000001.10 - 11710561	Jul 12, 2019 (153)
149	GO Exome Sequencing Project	NC_000001.10 - 11710561	Oct 11, 2018 (152)
150	HGDP-CEPH-db Supplement 1	NC_000001.9 - 11633148	Apr 25, 2020 (154)
151	HapMap	NC_000001.11 - 11650504	Apr 25, 2020 (154)
152	KOREAN population from KRGDB	NC_000001.10 - 11710561	Apr 25, 2020 (154)
153	Korean Genome Project	NC_000001.11 - 11650504	Apr 25, 2020 (154)
154	Medical Genome Project healthy controls from Spanish population	NC_000001.10 - 11710561	Apr 25, 2020 (154)
155	Northern Sweden	NC_000001.10 - 11710561	Jul 12, 2019 (153)
156	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000001.10 - 11710561	Apr 25, 2021 (155)
157	Qatari	NC_000001.10 - 11710561	Apr 25, 2020 (154)
158	SGDP_PRJ	NC_000001.10 - 11710561	Apr 25, 2020 (154)
159	Siberian	NC_000001.10 - 11710561	Apr 25, 2020 (154)
160	8.3KJPN	NC_000001.10 - 11710561	Apr 25, 2021 (155)
161	14KJPN	NC_000001.11 - 11650504	Oct 12, 2022 (156)
162	TopMed	NC_000001.11 - 11650504	Apr 25, 2021 (155)
163	UK 10K study - Twins	NC_000001.10 - 11710561	Oct 11, 2018 (152)
164	A Vietnamese Genetic Variation Database	NC_000001.10 - 11710561	Jul 12, 2019 (153)
165	ALFA	NC_000001.11 - 11650504	Apr 25, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs1055561	Apr 12, 2001 (94)
rs3170621	Jul 03, 2002 (106)
rs17342213	Mar 11, 2006 (126)
rs17349907	Mar 11, 2006 (126)
rs60441174	May 26, 2008 (130)
rs386623787	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
263169, ss3893085775	NC_000001.10:11710560:T:A	NC_000001.11:11650503:T:A	(self)
ss3638890000, ss3639441870	NC_000001.8:11644826:T:G	NC_000001.11:11650503:T:G	(self)
2469, ss118499144, ss198022865, ss217314416, ss217390856, ss217392087, ss217399977, ss217405871, ss217410518, ss217410996, ss275714798, ss481950922, ss491584486, ss825631980, ss1584217171, ss1712311346, ss3642751304, ss3847324577	NC_000001.9:11633147:T:G	NC_000001.11:11650503:T:G	(self)
373103, 194341, 140571, 4481059, 1101, 1390368, 133482, 18525, 263169, 4899, 77978, 4624, 100685, 217660, 57473, 461764, 194341, 40545, ss218237779, ss230427141, ss238142409, ss341932891, ss481984517, ss482939593, ss485769124, ss489720754, ss491286197, ss537617591, ss553800307, ss647576793, ss778644452, ss783330387, ss784282108, ss832592155, ss833188672, ss834102186, ss974433201, ss974858980, ss1067416122, ss1067671660, ss1289696571, ss1573888548, ss1584004640, ss1599555197, ss1642549230, ss1685301788, ss1710888147, ss1751865786, ss1793909905, ss1918058755, ss2019543203, ss2147541119, ss2624287967, ss2632477777, ss2697437711, ss2710665674, ss2731117153, ss2746214301, ss2751661248, ss2984845249, ss2986301573, ss3343318938, ss3626026720, ss3630516181, ss3632880852, ss3633574679, ss3634306931, ss3635268803, ss3635983063, ss3637019170, ss3637737437, ss3640014295, ss3646221271, ss3653618881, ss3654402323, ss3726793113, ss3744607913, ss3745833591, ss3772109525, ss3823559797, ss3825553341, ss3826024974, ss3848200680, ss3893085775, ss3983915807, ss3983915808, ss3984778697, ss3986008466, ss3986098831, ss4016893418, ss5142492457, ss5314593150, ss5316773859, ss5623987353, ss5624932091, ss5799407201, ss5799475119, ss5800077774, ss5831544693, ss5848247877, ss5936759062	NC_000001.10:11710560:T:G	NC_000001.11:11650503:T:G	(self)
479024, 2597359, 13870, 210063, 637408, 2945098, 315023623, ss2160077029, ss3023535795, ss3686170331, ss3798853849, ss3943832062, ss4439338763, ss5236864153, ss5241189044, ss5442391673, ss5512953089, ss5666800304, ss5800326038, ss5848784965, ss5907058261	NC_000001.11:11650503:T:G	NC_000001.11:11650503:T:G	(self)
ss11719, ss1343940, ss4397096, ss24780393, ss24790484, ss65732162, ss66695693, ss67936581, ss68054341, ss71619073, ss75589698, ss79301462, ss83349217, ss86341819, ss98278251, ss123022319, ss154504086, ss154639515, ss159677965, ss159696078, ss161003807, ss172487149, ss174877960	NT_021937.19:7715292:T:G	NC_000001.11:11650503:T:G	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

1 citation for rs9614

PMID	Title	Author	Year	Journal
28341977	Genetic Analysis of FBXO2, FBXO6, FBXO12, and FBXO41 Variants in Han Chinese Patients with Sporadic Parkinson's Disease.	Yuan L et al.	2017	Neuroscience bulletin

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs9614