Name: rs1505034
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.

rs1505034

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr5:15773925 (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: G>C / G>T
Variation Type: SNV Single Nucleotide Variation
Frequency: G=0.464298 (122895/264690, TOPMED)
G=0.437745 (85278/194812, ALFA)
G=0.36715 (10375/28258, 14KJPN) (+ 19 more)
G=0.36581 (6131/16760, 8.3KJPN)
G=0.4413 (2826/6404, 1000G_30x)
G=0.4938 (2212/4480, Estonian)
G=0.4349 (1676/3854, ALSPAC)
G=0.4156 (1541/3708, TWINSUK)
G=0.3307 (969/2930, KOREAN)
G=0.4765 (993/2084, HGDP_Stanford)
G=0.4495 (846/1882, HapMap)
G=0.3575 (655/1832, Korea1K)
G=0.4683 (532/1136, Daghestan)
G=0.405 (404/998, GoNL)
G=0.417 (250/600, NorthernSweden)
G=0.302 (128/424, SGDP_PRJ)
G=0.500 (108/216, Qatari)
T=0.500 (108/216, Qatari)
G=0.322 (67/208, Vietnamese)
G=0.45 (26/58, Ancient Sardinia)
G=0.38 (16/42, Siberian)
T=0.40 (16/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: FBXL7 : Intron Variant
Publications: 0 citations
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	194812	G=0.437745	C=0.000000, T=0.562255
European	Sub	166664	G=0.428941	C=0.000000, T=0.571059
African	Sub	7756	G=0.5971	C=0.0000, T=0.4029
African Others	Sub	268	G=0.679	C=0.000, T=0.321
African American	Sub	7488	G=0.5942	C=0.0000, T=0.4058
Asian	Sub	614	G=0.363	C=0.000, T=0.637
East Asian	Sub	484	G=0.351	C=0.000, T=0.649
Other Asian	Sub	130	G=0.408	C=0.000, T=0.592
Latin American 1	Sub	770	G=0.523	C=0.000, T=0.477
Latin American 2	Sub	7594	G=0.4704	C=0.0000, T=0.5296
South Asian	Sub	4972	G=0.4049	C=0.0000, T=0.5951
Other	Sub	6442	G=0.4575	C=0.0000, T=0.5425

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	G=0.464298	T=0.535702
Allele Frequency Aggregator	Total	Global	194812	G=0.437745	C=0.000000, T=0.562255
Allele Frequency Aggregator	European	Sub	166664	G=0.428941	C=0.000000, T=0.571059
Allele Frequency Aggregator	African	Sub	7756	G=0.5971	C=0.0000, T=0.4029
Allele Frequency Aggregator	Latin American 2	Sub	7594	G=0.4704	C=0.0000, T=0.5296
Allele Frequency Aggregator	Other	Sub	6442	G=0.4575	C=0.0000, T=0.5425
Allele Frequency Aggregator	South Asian	Sub	4972	G=0.4049	C=0.0000, T=0.5951
Allele Frequency Aggregator	Latin American 1	Sub	770	G=0.523	C=0.000, T=0.477
Allele Frequency Aggregator	Asian	Sub	614	G=0.363	C=0.000, T=0.637
14KJPN	JAPANESE	Study-wide	28258	G=0.36715	T=0.63285
8.3KJPN	JAPANESE	Study-wide	16760	G=0.36581	T=0.63419
1000Genomes_30x	Global	Study-wide	6404	G=0.4413	C=0.0002, T=0.5586
1000Genomes_30x	African	Sub	1786	G=0.5504	C=0.0000, T=0.4496
1000Genomes_30x	Europe	Sub	1266	G=0.4179	C=0.0000, T=0.5821
1000Genomes_30x	South Asian	Sub	1202	G=0.3710	C=0.0000, T=0.6290
1000Genomes_30x	East Asian	Sub	1170	G=0.3419	C=0.0000, T=0.6581
1000Genomes_30x	American	Sub	980	G=0.478	C=0.001, T=0.521
Genetic variation in the Estonian population	Estonian	Study-wide	4480	G=0.4938	T=0.5062
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.4349	T=0.5651
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.4156	T=0.5844
KOREAN population from KRGDB	KOREAN	Study-wide	2930	G=0.3307	T=0.6693
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	G=0.4765	T=0.5235
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	G=0.349	T=0.651
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	G=0.502	T=0.498
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	G=0.431	T=0.569
HGDP-CEPH-db Supplement 1	Europe	Sub	320	G=0.394	T=0.606
HGDP-CEPH-db Supplement 1	Africa	Sub	242	G=0.719	T=0.281
HGDP-CEPH-db Supplement 1	America	Sub	216	G=0.542	T=0.458
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	G=0.74	T=0.26
HapMap	Global	Study-wide	1882	G=0.4495	T=0.5505
HapMap	American	Sub	764	G=0.399	T=0.601
HapMap	African	Sub	688	G=0.547	T=0.453
HapMap	Asian	Sub	254	G=0.394	T=0.606
HapMap	Europe	Sub	176	G=0.369	T=0.631
Korean Genome Project	KOREAN	Study-wide	1832	G=0.3575	T=0.6425
Genome-wide autozygosity in Daghestan	Global	Study-wide	1136	G=0.4683	T=0.5317
Genome-wide autozygosity in Daghestan	Daghestan	Sub	628	G=0.532	T=0.468
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	G=0.424	T=0.576
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	G=0.393	T=0.607
Genome-wide autozygosity in Daghestan	Europe	Sub	108	G=0.454	T=0.546
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	G=0.26	T=0.74
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	G=0.42	T=0.58
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	G=0.405	T=0.595
Northern Sweden	ACPOP	Study-wide	600	G=0.417	T=0.583
SGDP_PRJ	Global	Study-wide	424	G=0.302	T=0.698
Qatari	Global	Study-wide	216	G=0.500	T=0.500
A Vietnamese Genetic Variation Database	Global	Study-wide	208	G=0.322	T=0.678
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	58	G=0.45	T=0.55
Siberian	Global	Study-wide	42	G=0.38	T=0.62
The Danish reference pan genome	Danish	Study-wide	40	G=0.60	T=0.40

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 5	NC_000005.10:g.15773925G>C
GRCh38.p14 chr 5	NC_000005.10:g.15773925G>T
GRCh37.p13 chr 5	NC_000005.9:g.15774034G>C
GRCh37.p13 chr 5	NC_000005.9:g.15774034G>T

Gene: FBXL7, F-box and leucine rich repeat protein 7 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
FBXL7 transcript variant 2	NM_001278317.2:c.-14-1539… NM_001278317.2:c.-14-153965G>C	N/A	Intron Variant
FBXL7 transcript variant 1	NM_012304.5:c.128-153965G… NM_012304.5:c.128-153965G>C	N/A	Intron Variant
FBXL7 transcript variant X3	XM_011513998.2:c.-91-6085… XM_011513998.2:c.-91-60852G>C	N/A	Intron Variant
FBXL7 transcript variant X1	XM_017009262.3:c.113-1539… XM_017009262.3:c.113-153965G>C	N/A	Intron Variant
FBXL7 transcript variant X2	XM_047417000.1:c.-14-1539… XM_047417000.1:c.-14-153965G>C	N/A	Intron 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	G=	C	T
GRCh38.p14 chr 5	NC_000005.10:g.15773925=	NC_000005.10:g.15773925G>C	NC_000005.10:g.15773925G>T
GRCh37.p13 chr 5	NC_000005.9:g.15774034=	NC_000005.9:g.15774034G>C	NC_000005.9:g.15774034G>T
FBXL7 transcript variant 2	NM_001278317.1:c.-14-153965=	NM_001278317.1:c.-14-153965G>C	NM_001278317.1:c.-14-153965G>T
FBXL7 transcript variant 2	NM_001278317.2:c.-14-153965=	NM_001278317.2:c.-14-153965G>C	NM_001278317.2:c.-14-153965G>T
FBXL7 transcript variant 1	NM_012304.4:c.128-153965=	NM_012304.4:c.128-153965G>C	NM_012304.4:c.128-153965G>T
FBXL7 transcript variant 1	NM_012304.5:c.128-153965=	NM_012304.5:c.128-153965G>C	NM_012304.5:c.128-153965G>T
FBXL7 transcript variant X1	XM_005248273.1:c.113-153965=	XM_005248273.1:c.113-153965G>C	XM_005248273.1:c.113-153965G>T
FBXL7 transcript variant X3	XM_011513998.2:c.-91-60852=	XM_011513998.2:c.-91-60852G>C	XM_011513998.2:c.-91-60852G>T
FBXL7 transcript variant X1	XM_017009262.3:c.113-153965=	XM_017009262.3:c.113-153965G>C	XM_017009262.3:c.113-153965G>T
FBXL7 transcript variant X2	XM_047417000.1:c.-14-153965=	XM_047417000.1:c.-14-153965G>C	XM_047417000.1:c.-14-153965G>T

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, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss2336872	Oct 23, 2000 (88)
2	SC_JCM	ss4141321	Nov 05, 2001 (101)
3	PERLEGEN	ss24667076	Sep 20, 2004 (123)
4	ABI	ss44586505	Mar 14, 2006 (126)
5	ILLUMINA	ss66553729	Nov 30, 2006 (127)
6	ILLUMINA	ss67120092	Nov 30, 2006 (127)
7	ILLUMINA	ss67458215	Nov 30, 2006 (127)
8	ILLUMINA	ss70438473	May 17, 2007 (127)
9	ILLUMINA	ss70625939	May 27, 2008 (130)
10	ILLUMINA	ss71175294	May 17, 2007 (127)
11	ILLUMINA	ss75743910	Dec 06, 2007 (129)
12	AFFY	ss76804785	Dec 06, 2007 (129)
13	KRIBB_YJKIM	ss83806062	Dec 16, 2007 (130)
14	HGSV	ss84208521	Dec 16, 2007 (130)
15	BCMHGSC_JDW	ss93004503	Mar 24, 2008 (129)
16	BGI	ss104171053	Dec 01, 2009 (131)
17	1000GENOMES	ss108832318	Jan 23, 2009 (130)
18	1000GENOMES	ss111475422	Jan 25, 2009 (130)
19	ILLUMINA-UK	ss116490630	Feb 14, 2009 (130)
20	ILLUMINA	ss120244293	Dec 01, 2009 (131)
21	ILLUMINA	ss121726893	Dec 01, 2009 (131)
22	ENSEMBL	ss142891040	Dec 01, 2009 (131)
23	ILLUMINA	ss153478168	Dec 01, 2009 (131)
24	GMI	ss155087029	Dec 01, 2009 (131)
25	ILLUMINA	ss159277988	Dec 01, 2009 (131)
26	ILLUMINA	ss160363788	Dec 01, 2009 (131)
27	COMPLETE_GENOMICS	ss162041635	Jul 04, 2010 (132)
28	COMPLETE_GENOMICS	ss164320011	Jul 04, 2010 (132)
29	COMPLETE_GENOMICS	ss166207474	Jul 04, 2010 (132)
30	ILLUMINA	ss170584417	Jul 04, 2010 (132)
31	ILLUMINA	ss172546473	Jul 04, 2010 (132)
32	BUSHMAN	ss199925643	Jul 04, 2010 (132)
33	BCM-HGSC-SUB	ss207018272	Jul 04, 2010 (132)
34	1000GENOMES	ss221537219	Jul 14, 2010 (132)
35	1000GENOMES	ss232842252	Jul 14, 2010 (132)
36	1000GENOMES	ss240037184	Jul 15, 2010 (132)
37	ILLUMINA	ss244256939	Jul 04, 2010 (132)
38	BL	ss253253087	May 09, 2011 (134)
39	GMI	ss278182403	May 04, 2012 (137)
40	GMI	ss285125882	Apr 25, 2013 (138)
41	ILLUMINA	ss480006138	May 04, 2012 (137)
42	ILLUMINA	ss480014791	May 04, 2012 (137)
43	ILLUMINA	ss480672735	Sep 08, 2015 (146)
44	ILLUMINA	ss484801135	May 04, 2012 (137)
45	ILLUMINA	ss536883726	Sep 08, 2015 (146)
46	TISHKOFF	ss558229987	Apr 25, 2013 (138)
47	SSMP	ss652074018	Apr 25, 2013 (138)
48	ILLUMINA	ss778810173	Sep 08, 2015 (146)
49	ILLUMINA	ss782847198	Sep 08, 2015 (146)
50	ILLUMINA	ss783811788	Sep 08, 2015 (146)
51	ILLUMINA	ss825407457	Apr 01, 2015 (144)
52	ILLUMINA	ss832101015	Sep 08, 2015 (146)
53	ILLUMINA	ss832790136	Jul 13, 2019 (153)
54	ILLUMINA	ss834270427	Sep 08, 2015 (146)
55	EVA-GONL	ss981286542	Aug 21, 2014 (142)
56	JMKIDD_LAB	ss1072421166	Aug 21, 2014 (142)
57	HAMMER_LAB	ss1397406202	Sep 08, 2015 (146)
58	DDI	ss1430258611	Apr 01, 2015 (144)
59	EVA_GENOME_DK	ss1581027662	Apr 01, 2015 (144)
60	EVA_DECODE	ss1590804982	Apr 01, 2015 (144)
61	EVA_UK10K_ALSPAC	ss1612357404	Apr 01, 2015 (144)
62	EVA_UK10K_TWINSUK	ss1655351437	Apr 01, 2015 (144)
63	EVA_SVP	ss1712747034	Apr 01, 2015 (144)
64	ILLUMINA	ss1752559195	Sep 08, 2015 (146)
65	HAMMER_LAB	ss1803121107	Sep 08, 2015 (146)
66	WEILL_CORNELL_DGM	ss1924547963	Feb 12, 2016 (147)
67	GENOMED	ss1970022687	Jul 19, 2016 (147)
68	JJLAB	ss2022872052	Sep 14, 2016 (149)
69	USC_VALOUEV	ss2151021143	Dec 20, 2016 (150)
70	HUMAN_LONGEVITY	ss2271686405	Dec 20, 2016 (150)
71	SYSTEMSBIOZJU	ss2625935021	Nov 08, 2017 (151)
72	ILLUMINA	ss2634250473	Nov 08, 2017 (151)
73	GRF	ss2706549093	Nov 08, 2017 (151)
74	GNOMAD	ss2821559903	Nov 08, 2017 (151)
75	SWEGEN	ss2996494474	Nov 08, 2017 (151)
76	BIOINF_KMB_FNS_UNIBA	ss3025220565	Nov 08, 2017 (151)
77	CSHL	ss3346259823	Nov 08, 2017 (151)
78	ILLUMINA	ss3629185856	Oct 12, 2018 (152)
79	ILLUMINA	ss3632179062	Oct 12, 2018 (152)
80	ILLUMINA	ss3633366795	Oct 12, 2018 (152)
81	ILLUMINA	ss3634087090	Oct 12, 2018 (152)
82	ILLUMINA	ss3634992730	Oct 12, 2018 (152)
83	ILLUMINA	ss3635769294	Oct 12, 2018 (152)
84	ILLUMINA	ss3636702294	Oct 12, 2018 (152)
85	ILLUMINA	ss3637521897	Oct 12, 2018 (152)
86	ILLUMINA	ss3638540557	Oct 12, 2018 (152)
87	ILLUMINA	ss3639273001	Oct 12, 2018 (152)
88	ILLUMINA	ss3639659335	Oct 12, 2018 (152)
89	ILLUMINA	ss3640700023	Oct 12, 2018 (152)
90	ILLUMINA	ss3643487553	Oct 12, 2018 (152)
91	EGCUT_WGS	ss3664390576	Jul 13, 2019 (153)
92	EVA_DECODE	ss3714176678	Jul 13, 2019 (153)
93	ACPOP	ss3732121492	Jul 13, 2019 (153)
94	ILLUMINA	ss3745292866	Jul 13, 2019 (153)
95	EVA	ss3763113662	Jul 13, 2019 (153)
96	ILLUMINA	ss3772787209	Jul 13, 2019 (153)
97	PACBIO	ss3785034947	Jul 13, 2019 (153)
98	PACBIO	ss3790451841	Jul 13, 2019 (153)
99	PACBIO	ss3795328444	Jul 13, 2019 (153)
100	KHV_HUMAN_GENOMES	ss3806279978	Jul 13, 2019 (153)
101	EVA	ss3829113024	Apr 26, 2020 (154)
102	EVA	ss3838020367	Apr 26, 2020 (154)
103	EVA	ss3843460367	Apr 26, 2020 (154)
104	HGDP	ss3847782836	Apr 26, 2020 (154)
105	SGDP_PRJ	ss3861293026	Apr 26, 2020 (154)
106	KRGDB	ss3907739582	Apr 26, 2020 (154)
107	KOGIC	ss3956160383	Apr 26, 2020 (154)
108	EVA	ss3985127672	Apr 26, 2021 (155)
109	TOPMED	ss4650859665	Apr 26, 2021 (155)
110	TOMMO_GENOMICS	ss5170541044	Apr 26, 2021 (155)
111	1000G_HIGH_COVERAGE	ss5263004841	Oct 13, 2022 (156)
112	EVA	ss5315035051	Oct 13, 2022 (156)
113	EVA	ss5355895169	Oct 13, 2022 (156)
114	HUGCELL_USP	ss5461340412	Oct 13, 2022 (156)
115	HUGCELL_USP	ss5461340413	Oct 13, 2022 (156)
116	1000G_HIGH_COVERAGE	ss5546121065	Oct 13, 2022 (156)
117	SANFORD_IMAGENETICS	ss5637259367	Oct 13, 2022 (156)
118	TOMMO_GENOMICS	ss5706259302	Oct 13, 2022 (156)
119	EVA	ss5799642423	Oct 13, 2022 (156)
120	YY_MCH	ss5806052565	Oct 13, 2022 (156)
121	EVA	ss5834570290	Oct 13, 2022 (156)
122	EVA	ss5854700485	Oct 13, 2022 (156)
123	EVA	ss5893144658	Oct 13, 2022 (156)
124	EVA	ss5965676769	Oct 13, 2022 (156)
125	1000Genomes_30x	NC_000005.10 - 15773925	Oct 13, 2022 (156)
126	The Avon Longitudinal Study of Parents and Children	NC_000005.9 - 15774034	Oct 12, 2018 (152)
127	Genome-wide autozygosity in Daghestan	NC_000005.8 - 15827034	Apr 26, 2020 (154)
128	Genetic variation in the Estonian population	NC_000005.9 - 15774034	Oct 12, 2018 (152)
129	The Danish reference pan genome	NC_000005.9 - 15774034	Apr 26, 2020 (154)
130	gnomAD - Genomes Submission ignored due to conflicting rows: Row 180966556 (NC_000005.10:15773924:G:C 19/139928) Row 180966557 (NC_000005.10:15773924:G:T 74650/139854)	-	Apr 26, 2021 (155)
131	gnomAD - Genomes Submission ignored due to conflicting rows: Row 180966556 (NC_000005.10:15773924:G:C 19/139928) Row 180966557 (NC_000005.10:15773924:G:T 74650/139854)	-	Apr 26, 2021 (155)
132	Genome of the Netherlands Release 5	NC_000005.9 - 15774034	Apr 26, 2020 (154)
133	HGDP-CEPH-db Supplement 1	NC_000005.8 - 15827034	Apr 26, 2020 (154)
134	HapMap	NC_000005.10 - 15773925	Apr 26, 2020 (154)
135	KOREAN population from KRGDB	NC_000005.9 - 15774034	Apr 26, 2020 (154)
136	Korean Genome Project	NC_000005.10 - 15773925	Apr 26, 2020 (154)
137	Northern Sweden	NC_000005.9 - 15774034	Jul 13, 2019 (153)
138	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000005.9 - 15774034	Apr 26, 2021 (155)
139	Qatari	NC_000005.9 - 15774034	Apr 26, 2020 (154)
140	SGDP_PRJ	NC_000005.9 - 15774034	Apr 26, 2020 (154)
141	Siberian	NC_000005.9 - 15774034	Apr 26, 2020 (154)
142	8.3KJPN	NC_000005.9 - 15774034	Apr 26, 2021 (155)
143	14KJPN	NC_000005.10 - 15773925	Oct 13, 2022 (156)
144	TopMed	NC_000005.10 - 15773925	Apr 26, 2021 (155)
145	UK 10K study - Twins	NC_000005.9 - 15774034	Oct 12, 2018 (152)
146	A Vietnamese Genetic Variation Database	NC_000005.9 - 15774034	Jul 13, 2019 (153)
147	ALFA	NC_000005.10 - 15773925	Apr 26, 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)
rs17524436	Oct 07, 2004 (123)
rs61686090	May 27, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss2821559903	NC_000005.9:15774033:G:C	NC_000005.10:15773924:G:C	(self)
33647000, 2142737793, ss2271686405, ss5461340413, ss5546121065	NC_000005.10:15773924:G:C	NC_000005.10:15773924:G:C	(self)
381336, 460728, ss84208521, ss93004503, ss108832318, ss111475422, ss116490630, ss162041635, ss164320011, ss166207474, ss199925643, ss207018272, ss253253087, ss278182403, ss285125882, ss480006138, ss825407457, ss1397406202, ss1590804982, ss1712747034, ss3639273001, ss3639659335, ss3643487553, ss3847782836	NC_000005.8:15827033:G:T	NC_000005.10:15773924:G:T	(self)
14256259, 10128824, 7192601, 6327098, 14916976, 5406357, 353599, 6589893, 13310006, 3537497, 28510351, 14256259, 3163393, ss221537219, ss232842252, ss240037184, ss480014791, ss480672735, ss484801135, ss536883726, ss558229987, ss652074018, ss778810173, ss782847198, ss783811788, ss832101015, ss832790136, ss834270427, ss981286542, ss1072421166, ss1430258611, ss1581027662, ss1612357404, ss1655351437, ss1752559195, ss1803121107, ss1924547963, ss1970022687, ss2022872052, ss2151021143, ss2625935021, ss2634250473, ss2706549093, ss2821559903, ss2996494474, ss3346259823, ss3629185856, ss3632179062, ss3633366795, ss3634087090, ss3634992730, ss3635769294, ss3636702294, ss3637521897, ss3638540557, ss3640700023, ss3664390576, ss3732121492, ss3745292866, ss3763113662, ss3772787209, ss3785034947, ss3790451841, ss3795328444, ss3829113024, ss3838020367, ss3861293026, ss3907739582, ss3985127672, ss5170541044, ss5315035051, ss5355895169, ss5637259367, ss5799642423, ss5834570290, ss5965676769	NC_000005.9:15774033:G:T	NC_000005.10:15773924:G:T	(self)
33647000, 2816806, 12538384, 40096406, 488237222, 2142737793, ss2271686405, ss3025220565, ss3714176678, ss3806279978, ss3843460367, ss3956160383, ss4650859665, ss5263004841, ss5461340412, ss5546121065, ss5706259302, ss5806052565, ss5854700485, ss5893144658	NC_000005.10:15773924:G:T	NC_000005.10:15773924:G:T	(self)
ss2336872, ss4141321, ss24667076, ss44586505, ss66553729, ss67120092, ss67458215, ss70438473, ss70625939, ss71175294, ss75743910, ss76804785, ss83806062, ss104171053, ss120244293, ss121726893, ss142891040, ss153478168, ss155087029, ss159277988, ss160363788, ss170584417, ss172546473, ss244256939	NT_006576.16:15764033:G:T	NC_000005.10:15773924:G:T	(self)

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

No publications for rs1505034

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
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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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1505034