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dbSNP Short Genetic Variations

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 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr1:11650504 (GRCh38.p13) 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) (+ 21 more)
G=0.194793 (27310/140200, GnomAD)
G=0.26117 (22875/87586, ExAC)
G=0.44069 (7385/16758, 8.3KJPN)
G=0.18339 (2383/12994, GO-ESP)
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
Help

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.p13 chr 1 NC_000001.11:g.11650504T>A
GRCh38.p13 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
Help

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

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: 20201027095038
Population Group Sample Size Ref Allele Alt Allele
Total Global 250840 T=0.802001 G=0.197999
European Sub 215914 T=0.804098 G=0.195902
African Sub 7516 T=0.8249 G=0.1751
African Others Sub 270 T=0.841 G=0.159
African American Sub 7246 T=0.8243 G=0.1757
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 13456 T=0.79838 G=0.20162


Help

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").

Download
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
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 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
Help

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.p13 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
Help

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#.

124 SubSNP, 24 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 TOPMED ss2322234737 Dec 20, 2016 (150)
75 SYSTEMSBIOZJU ss2624287967 Nov 08, 2017 (151)
76 ILLUMINA ss2632477777 Nov 08, 2017 (151)
77 GRF ss2697437711 Nov 08, 2017 (151)
78 ILLUMINA ss2710665674 Nov 08, 2017 (151)
79 GNOMAD ss2731117153 Nov 08, 2017 (151)
80 GNOMAD ss2746214301 Nov 08, 2017 (151)
81 GNOMAD ss2751661248 Nov 08, 2017 (151)
82 AFFY ss2984845249 Nov 08, 2017 (151)
83 SWEGEN ss2986301573 Nov 08, 2017 (151)
84 BIOINF_KMB_FNS_UNIBA ss3023535795 Nov 08, 2017 (151)
85 TOPMED ss3068682860 Nov 08, 2017 (151)
86 CSHL ss3343318938 Nov 08, 2017 (151)
87 ILLUMINA ss3626026720 Oct 11, 2018 (152)
88 ILLUMINA ss3630516181 Oct 11, 2018 (152)
89 ILLUMINA ss3632880852 Oct 11, 2018 (152)
90 ILLUMINA ss3633574679 Oct 11, 2018 (152)
91 ILLUMINA ss3634306931 Oct 11, 2018 (152)
92 ILLUMINA ss3635268803 Oct 11, 2018 (152)
93 ILLUMINA ss3635983063 Oct 11, 2018 (152)
94 ILLUMINA ss3637019170 Oct 11, 2018 (152)
95 ILLUMINA ss3637737437 Oct 11, 2018 (152)
96 ILLUMINA ss3638890000 Oct 11, 2018 (152)
97 ILLUMINA ss3639441870 Oct 11, 2018 (152)
98 ILLUMINA ss3640014295 Oct 11, 2018 (152)
99 ILLUMINA ss3642751304 Oct 11, 2018 (152)
100 OMUKHERJEE_ADBS ss3646221271 Oct 11, 2018 (152)
101 ILLUMINA ss3653618881 Oct 11, 2018 (152)
102 EGCUT_WGS ss3654402323 Jul 12, 2019 (153)
103 EVA_DECODE ss3686170331 Jul 12, 2019 (153)
104 ACPOP ss3726793113 Jul 12, 2019 (153)
105 ILLUMINA ss3744607913 Jul 12, 2019 (153)
106 EVA ss3745833591 Jul 12, 2019 (153)
107 ILLUMINA ss3772109525 Jul 12, 2019 (153)
108 KHV_HUMAN_GENOMES ss3798853849 Jul 12, 2019 (153)
109 EVA ss3823559797 Apr 25, 2020 (154)
110 EVA ss3825553341 Apr 25, 2020 (154)
111 EVA ss3826024974 Apr 25, 2020 (154)
112 HGDP ss3847324577 Apr 25, 2020 (154)
113 SGDP_PRJ ss3848200680 Apr 25, 2020 (154)
114 KRGDB ss3893085775 Apr 25, 2020 (154)
115 KOGIC ss3943832062 Apr 25, 2020 (154)
116 FSA-LAB ss3983915807 Apr 25, 2021 (155)
117 FSA-LAB ss3983915808 Apr 25, 2021 (155)
118 EVA ss3984778697 Apr 25, 2021 (155)
119 EVA ss3986008466 Apr 25, 2021 (155)
120 EVA ss3986098831 Apr 25, 2021 (155)
121 EVA ss4016893418 Apr 25, 2021 (155)
122 TOPMED ss4439338763 Apr 25, 2021 (155)
123 TOMMO_GENOMICS ss5142492457 Apr 25, 2021 (155)
124 EVA ss5236864153 Apr 25, 2021 (155)
125 1000Genomes NC_000001.10 - 11710561 Oct 11, 2018 (152)
126 The Avon Longitudinal Study of Parents and Children NC_000001.10 - 11710561 Oct 11, 2018 (152)
127 Genetic variation in the Estonian population NC_000001.10 - 11710561 Oct 11, 2018 (152)
128 ExAC NC_000001.10 - 11710561 Oct 11, 2018 (152)
129 FINRISK NC_000001.10 - 11710561 Apr 25, 2020 (154)
130 The Danish reference pan genome NC_000001.10 - 11710561 Apr 25, 2020 (154)
131 gnomAD - Genomes NC_000001.11 - 11650504 Apr 25, 2021 (155)
132 gnomAD - Exomes NC_000001.10 - 11710561 Jul 12, 2019 (153)
133 GO Exome Sequencing Project NC_000001.10 - 11710561 Oct 11, 2018 (152)
134 HGDP-CEPH-db Supplement 1 NC_000001.9 - 11633148 Apr 25, 2020 (154)
135 HapMap NC_000001.11 - 11650504 Apr 25, 2020 (154)
136 KOREAN population from KRGDB NC_000001.10 - 11710561 Apr 25, 2020 (154)
137 Korean Genome Project NC_000001.11 - 11650504 Apr 25, 2020 (154)
138 Medical Genome Project healthy controls from Spanish population NC_000001.10 - 11710561 Apr 25, 2020 (154)
139 Northern Sweden NC_000001.10 - 11710561 Jul 12, 2019 (153)
140 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000001.10 - 11710561 Apr 25, 2021 (155)
141 Qatari NC_000001.10 - 11710561 Apr 25, 2020 (154)
142 SGDP_PRJ NC_000001.10 - 11710561 Apr 25, 2020 (154)
143 Siberian NC_000001.10 - 11710561 Apr 25, 2020 (154)
144 8.3KJPN NC_000001.10 - 11710561 Apr 25, 2021 (155)
145 TopMed NC_000001.11 - 11650504 Apr 25, 2021 (155)
146 UK 10K study - Twins NC_000001.10 - 11710561 Oct 11, 2018 (152)
147 A Vietnamese Genetic Variation Database NC_000001.10 - 11710561 Jul 12, 2019 (153)
148 ALFA NC_000001.11 - 11650504 Apr 25, 2021 (155)
Help

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, ss2322234737, 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 NC_000001.10:11710560:T:G NC_000001.11:11650503:T:G (self)
2597359, 13870, 210063, 1853049, 2945098, 315023623, ss2160077029, ss3023535795, ss3068682860, ss3686170331, ss3798853849, ss3943832062, ss4439338763, ss5236864153 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)
Help

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
Help

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.

Software version is: 2.0.1.post596+ae089ad