Name: rs575908
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.

rs575908

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:177930963 (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>C
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.309143 (81827/264690, TOPMED)
C=0.269976 (42275/156588, ALFA)
C=0.300698 (42111/140044, GnomAD) (+ 20 more)
T=0.37592 (10622/28256, 14KJPN)
T=0.37918 (6355/16760, 8.3KJPN)
C=0.3423 (2192/6404, 1000G_30x)
C=0.3504 (1755/5008, 1000G)
C=0.2565 (1149/4480, Estonian)
C=0.3072 (1184/3854, ALSPAC)
C=0.2848 (1056/3708, TWINSUK)
T=0.3546 (1039/2930, KOREAN)
C=0.3488 (727/2084, HGDP_Stanford)
C=0.3730 (699/1874, HapMap)
T=0.3876 (710/1832, Korea1K)
C=0.305 (304/998, GoNL)
C=0.392 (235/600, NorthernSweden)
T=0.331 (106/320, SGDP_PRJ)
C=0.190 (41/216, Qatari)
T=0.500 (106/212, Vietnamese)
C=0.500 (106/212, Vietnamese)
C=0.42 (17/40, GENOME_DK)
T=0.29 (11/38, Siberian)
C=0.20 (6/30, Ancient Sardinia)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CRYZL2P-SEC16B : Intron Variant
SEC16B : 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	156588	T=0.730024	A=0.000000, C=0.269976
European	Sub	138404	T=0.735846	A=0.000000, C=0.264154
African	Sub	4312	T=0.8077	A=0.0000, C=0.1923
African Others	Sub	174	T=0.816	A=0.000, C=0.184
African American	Sub	4138	T=0.8074	A=0.0000, C=0.1926
Asian	Sub	546	T=0.473	A=0.000, C=0.527
East Asian	Sub	426	T=0.444	A=0.000, C=0.556
Other Asian	Sub	120	T=0.575	A=0.000, C=0.425
Latin American 1	Sub	768	T=0.776	A=0.000, C=0.224
Latin American 2	Sub	6380	T=0.5893	A=0.0000, C=0.4107
South Asian	Sub	160	T=0.812	A=0.000, C=0.188
Other	Sub	6018	T=0.7049	A=0.0000, C=0.2951

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=0.690857	C=0.309143
Allele Frequency Aggregator	Total	Global	156588	T=0.730024	A=0.000000, C=0.269976
Allele Frequency Aggregator	European	Sub	138404	T=0.735846	A=0.000000, C=0.264154
Allele Frequency Aggregator	Latin American 2	Sub	6380	T=0.5893	A=0.0000, C=0.4107
Allele Frequency Aggregator	Other	Sub	6018	T=0.7049	A=0.0000, C=0.2951
Allele Frequency Aggregator	African	Sub	4312	T=0.8077	A=0.0000, C=0.1923
Allele Frequency Aggregator	Latin American 1	Sub	768	T=0.776	A=0.000, C=0.224
Allele Frequency Aggregator	Asian	Sub	546	T=0.473	A=0.000, C=0.527
Allele Frequency Aggregator	South Asian	Sub	160	T=0.812	A=0.000, C=0.188
gnomAD - Genomes	Global	Study-wide	140044	T=0.699302	C=0.300698
gnomAD - Genomes	European	Sub	75862	T=0.70980	C=0.29020
gnomAD - Genomes	African	Sub	41954	T=0.71297	C=0.28703
gnomAD - Genomes	American	Sub	13636	T=0.63919	C=0.36081
gnomAD - Genomes	Ashkenazi Jewish	Sub	3318	T=0.7797	C=0.2203
gnomAD - Genomes	East Asian	Sub	3126	T=0.4379	C=0.5621
gnomAD - Genomes	Other	Sub	2148	T=0.6993	C=0.3007
14KJPN	JAPANESE	Study-wide	28256	T=0.37592	C=0.62408
8.3KJPN	JAPANESE	Study-wide	16760	T=0.37918	C=0.62082
1000Genomes_30x	Global	Study-wide	6404	T=0.6577	C=0.3423
1000Genomes_30x	African	Sub	1786	T=0.7189	C=0.2811
1000Genomes_30x	Europe	Sub	1266	T=0.7046	C=0.2954
1000Genomes_30x	South Asian	Sub	1202	T=0.7238	C=0.2762
1000Genomes_30x	East Asian	Sub	1170	T=0.4581	C=0.5419
1000Genomes_30x	American	Sub	980	T=0.643	C=0.357
1000Genomes	Global	Study-wide	5008	T=0.6496	C=0.3504
1000Genomes	African	Sub	1322	T=0.7080	C=0.2920
1000Genomes	East Asian	Sub	1008	T=0.4573	C=0.5427
1000Genomes	Europe	Sub	1006	T=0.7068	C=0.2932
1000Genomes	South Asian	Sub	978	T=0.726	C=0.274
1000Genomes	American	Sub	694	T=0.627	C=0.373
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.7435	C=0.2565
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.6928	C=0.3072
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.7152	C=0.2848
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.3546	C=0.6454
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	T=0.6512	C=0.3488
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	T=0.438	C=0.562
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	T=0.725	C=0.275
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	T=0.829	C=0.171
HGDP-CEPH-db Supplement 1	Europe	Sub	320	T=0.809	C=0.191
HGDP-CEPH-db Supplement 1	Africa	Sub	242	T=0.785	C=0.215
HGDP-CEPH-db Supplement 1	America	Sub	216	T=0.199	C=0.801
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	T=0.96	C=0.04
HapMap	Global	Study-wide	1874	T=0.6270	C=0.3730
HapMap	American	Sub	766	T=0.599	C=0.401
HapMap	African	Sub	686	T=0.714	C=0.286
HapMap	Asian	Sub	250	T=0.400	C=0.600
HapMap	Europe	Sub	172	T=0.733	C=0.267
Korean Genome Project	KOREAN	Study-wide	1832	T=0.3876	C=0.6124
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.695	C=0.305
Northern Sweden	ACPOP	Study-wide	600	T=0.608	C=0.392
SGDP_PRJ	Global	Study-wide	320	T=0.331	C=0.669
Qatari	Global	Study-wide	216	T=0.810	C=0.190
A Vietnamese Genetic Variation Database	Global	Study-wide	212	T=0.500	C=0.500
The Danish reference pan genome	Danish	Study-wide	40	T=0.57	C=0.42
Siberian	Global	Study-wide	38	T=0.29	C=0.71
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	30	T=0.80	C=0.20

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.177930963T>A
GRCh38.p14 chr 1	NC_000001.11:g.177930963T>C
GRCh37.p13 chr 1	NC_000001.10:g.177900098T>A
GRCh37.p13 chr 1	NC_000001.10:g.177900098T>C

Gene: CRYZL2P-SEC16B, CRYZL2P-SEC16B readthrough (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CRYZL2P-SEC16B transcript variant 1	NM_001356505.2:c.3016-320… NM_001356505.2:c.3016-320A>T	N/A	Intron Variant
CRYZL2P-SEC16B transcript variant 2	NM_001356506.2:c.3016-320… NM_001356506.2:c.3016-320A>T	N/A	Intron Variant
CRYZL2P-SEC16B transcript variant 3	NR_151492.2:n.	N/A	Genic Downstream Transcript Variant

Gene: SEC16B, SEC16 homolog B, endoplasmic reticulum export factor (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SEC16B transcript variant 6	NM_001390833.1:c.3013-320… NM_001390833.1:c.3013-320A>T	N/A	Intron Variant
SEC16B transcript variant 4	NM_001390834.1:c.3019-320… NM_001390834.1:c.3019-320A>T	N/A	Intron Variant
SEC16B transcript variant 5	NM_001390835.1:c.3019-320… NM_001390835.1:c.3019-320A>T	N/A	Intron Variant
SEC16B transcript variant 1	NM_033127.4:c.3013-320A>T	N/A	Intron Variant
SEC16B transcript variant 2	NM_001356499.2:c.	N/A	Genic Downstream Transcript 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	C
GRCh38.p14 chr 1	NC_000001.11:g.177930963=	NC_000001.11:g.177930963T>A	NC_000001.11:g.177930963T>C
GRCh37.p13 chr 1	NC_000001.10:g.177900098=	NC_000001.10:g.177900098T>A	NC_000001.10:g.177900098T>C
CRYZL2P-SEC16B transcript variant 1	NM_001356505.2:c.3016-320=	NM_001356505.2:c.3016-320A>T	NM_001356505.2:c.3016-320A>G
CRYZL2P-SEC16B transcript variant 2	NM_001356506.2:c.3016-320=	NM_001356506.2:c.3016-320A>T	NM_001356506.2:c.3016-320A>G
SEC16B transcript variant 6	NM_001390833.1:c.3013-320=	NM_001390833.1:c.3013-320A>T	NM_001390833.1:c.3013-320A>G
SEC16B transcript variant 4	NM_001390834.1:c.3019-320=	NM_001390834.1:c.3019-320A>T	NM_001390834.1:c.3019-320A>G
SEC16B transcript variant 5	NM_001390835.1:c.3019-320=	NM_001390835.1:c.3019-320A>T	NM_001390835.1:c.3019-320A>G
SEC16B transcript	NM_033127.2:c.3013-320=	NM_033127.2:c.3013-320A>T	NM_033127.2:c.3013-320A>G
SEC16B transcript variant 1	NM_033127.4:c.3013-320=	NM_033127.4:c.3013-320A>T	NM_033127.4:c.3013-320A>G
SEC16B transcript variant X1	XM_005245573.1:c.3019-320=	XM_005245573.1:c.3019-320A>T	XM_005245573.1:c.3019-320A>G
SEC16B transcript variant X2	XM_005245574.1:c.3019-320=	XM_005245574.1:c.3019-320A>T	XM_005245574.1:c.3019-320A>G
SEC16B transcript variant X3	XM_005245575.1:c.1569-320=	XM_005245575.1:c.1569-320A>T	XM_005245575.1:c.1569-320A>G

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#.

109 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SC_JCM	ss747335	Aug 11, 2000 (83)
2	KWOK	ss1189664	Oct 05, 2000 (111)
3	KWOK	ss1957233	Oct 18, 2000 (111)
4	TSC-CSHL	ss3082276	Jun 15, 2001 (111)
5	CSHL-HAPMAP	ss16399161	Sep 28, 2016 (149)
6	SSAHASNP	ss20570351	Sep 28, 2016 (149)
7	ABI	ss41055886	Mar 15, 2006 (126)
8	HGSV	ss80753235	Dec 15, 2007 (130)
9	KRIBB_YJKIM	ss83487736	Dec 15, 2007 (130)
10	HUMANGENOME_JCVI	ss99264822	Feb 05, 2009 (130)
11	1000GENOMES	ss108728510	Jan 23, 2009 (130)
12	1000GENOMES	ss111393835	Jan 25, 2009 (130)
13	ILLUMINA-UK	ss119106811	Dec 01, 2009 (131)
14	ILLUMINA	ss160746166	Dec 01, 2009 (142)
15	COMPLETE_GENOMICS	ss164504709	Jul 04, 2010 (132)
16	COMPLETE_GENOMICS	ss165480583	Jul 04, 2010 (132)
17	COMPLETE_GENOMICS	ss167312311	Jul 04, 2010 (132)
18	BUSHMAN	ss199287254	Jul 04, 2010 (132)
19	1000GENOMES	ss218737192	Jul 14, 2010 (132)
20	1000GENOMES	ss230795709	Jul 14, 2010 (132)
21	1000GENOMES	ss238429417	Jul 15, 2010 (132)
22	BL	ss253629336	May 09, 2011 (134)
23	GMI	ss276114047	May 04, 2012 (137)
24	PJP	ss290670544	May 09, 2011 (134)
25	ILLUMINA	ss481157560	May 04, 2012 (142)
26	ILLUMINA	ss481179952	May 04, 2012 (142)
27	ILLUMINA	ss482168436	Sep 08, 2015 (146)
28	ILLUMINA	ss485373974	May 04, 2012 (142)
29	ILLUMINA	ss537314869	Sep 08, 2015 (146)
30	TISHKOFF	ss554888569	Apr 25, 2013 (138)
31	SSMP	ss648522541	Apr 25, 2013 (138)
32	ILLUMINA	ss778930840	Aug 21, 2014 (142)
33	ILLUMINA	ss783132582	Aug 21, 2014 (142)
34	ILLUMINA	ss784089019	Aug 21, 2014 (142)
35	ILLUMINA	ss832391497	Apr 01, 2015 (144)
36	ILLUMINA	ss833029068	Aug 21, 2014 (142)
37	ILLUMINA	ss833619896	Aug 21, 2014 (142)
38	ILLUMINA	ss834392381	Aug 21, 2014 (142)
39	EVA-GONL	ss975851808	Aug 21, 2014 (142)
40	JMKIDD_LAB	ss1068393312	Aug 21, 2014 (142)
41	1000GENOMES	ss1293573437	Aug 21, 2014 (142)
42	DDI	ss1426028596	Apr 01, 2015 (144)
43	EVA_GENOME_DK	ss1574499827	Apr 01, 2015 (144)
44	EVA_DECODE	ss1585241009	Apr 01, 2015 (144)
45	EVA_UK10K_ALSPAC	ss1601561063	Apr 01, 2015 (144)
46	EVA_UK10K_TWINSUK	ss1644555096	Apr 01, 2015 (144)
47	EVA_SVP	ss1712384420	Apr 01, 2015 (144)
48	ILLUMINA	ss1751883575	Sep 08, 2015 (146)
49	WEILL_CORNELL_DGM	ss1919089395	Feb 12, 2016 (147)
50	GENOMED	ss1966906627	Jul 19, 2016 (147)
51	JJLAB	ss2020060144	Sep 14, 2016 (149)
52	USC_VALOUEV	ss2148087632	Dec 20, 2016 (150)
53	HUMAN_LONGEVITY	ss2167862279	Dec 20, 2016 (150)
54	SYSTEMSBIOZJU	ss2624538529	Nov 08, 2017 (151)
55	ILLUMINA	ss2632597484	Nov 08, 2017 (151)
56	ILLUMINA	ss2635004792	Nov 08, 2017 (151)
57	GRF	ss2698068522	Nov 08, 2017 (151)
58	GNOMAD	ss2763150615	Nov 08, 2017 (151)
59	SWEGEN	ss2988011959	Nov 08, 2017 (151)
60	BIOINF_KMB_FNS_UNIBA	ss3023789311	Nov 08, 2017 (151)
61	CSHL	ss3343786575	Nov 08, 2017 (151)
62	ILLUMINA	ss3626248781	Oct 11, 2018 (152)
63	ILLUMINA	ss3630628969	Oct 11, 2018 (152)
64	ILLUMINA	ss3632916490	Oct 11, 2018 (152)
65	ILLUMINA	ss3633612111	Oct 11, 2018 (152)
66	ILLUMINA	ss3634360096	Oct 11, 2018 (152)
67	ILLUMINA	ss3635305421	Oct 11, 2018 (152)
68	ILLUMINA	ss3636039021	Oct 11, 2018 (152)
69	ILLUMINA	ss3637055931	Oct 11, 2018 (152)
70	ILLUMINA	ss3637798414	Oct 11, 2018 (152)
71	ILLUMINA	ss3638915247	Oct 11, 2018 (152)
72	ILLUMINA	ss3639769594	Oct 11, 2018 (152)
73	ILLUMINA	ss3640067450	Oct 11, 2018 (152)
74	ILLUMINA	ss3640989083	Oct 11, 2018 (152)
75	ILLUMINA	ss3641283145	Oct 11, 2018 (152)
76	ILLUMINA	ss3642806415	Oct 11, 2018 (152)
77	ILLUMINA	ss3643822893	Oct 11, 2018 (152)
78	URBANLAB	ss3646826470	Oct 11, 2018 (152)
79	EGCUT_WGS	ss3655959469	Jul 12, 2019 (153)
80	EVA_DECODE	ss3688095902	Jul 12, 2019 (153)
81	ACPOP	ss3727626517	Jul 12, 2019 (153)
82	ILLUMINA	ss3744660963	Jul 12, 2019 (153)
83	EVA	ss3747006188	Jul 12, 2019 (153)
84	ILLUMINA	ss3772161992	Jul 12, 2019 (153)
85	KHV_HUMAN_GENOMES	ss3800006315	Jul 12, 2019 (153)
86	EVA	ss3826507533	Apr 25, 2020 (154)
87	EVA	ss3836651210	Apr 25, 2020 (154)
88	EVA	ss3842061340	Apr 25, 2020 (154)
89	HGDP	ss3847355036	Apr 25, 2020 (154)
90	SGDP_PRJ	ss3850339611	Apr 25, 2020 (154)
91	KRGDB	ss3895590402	Apr 25, 2020 (154)
92	KOGIC	ss3945970835	Apr 25, 2020 (154)
93	EVA	ss3984836187	Apr 25, 2021 (155)
94	TOPMED	ss4474019318	Apr 25, 2021 (155)
95	TOMMO_GENOMICS	ss5147212586	Apr 25, 2021 (155)
96	1000G_HIGH_COVERAGE	ss5244852850	Oct 12, 2022 (156)
97	EVA	ss5314663478	Oct 12, 2022 (156)
98	HUGCELL_USP	ss5445382920	Oct 12, 2022 (156)
99	EVA	ss5506087198	Oct 12, 2022 (156)
100	1000G_HIGH_COVERAGE	ss5518465393	Oct 12, 2022 (156)
101	SANFORD_IMAGENETICS	ss5626910921	Oct 12, 2022 (156)
102	TOMMO_GENOMICS	ss5674621608	Oct 12, 2022 (156)
103	EVA	ss5799504132	Oct 12, 2022 (156)
104	YY_MCH	ss5801400462	Oct 12, 2022 (156)
105	EVA	ss5832887985	Oct 12, 2022 (156)
106	EVA	ss5849172700	Oct 12, 2022 (156)
107	EVA	ss5910889878	Oct 12, 2022 (156)
108	EVA	ss5938721382	Oct 12, 2022 (156)
109	EVA	ss5979296038	Oct 12, 2022 (156)
110	1000Genomes	NC_000001.10 - 177900098	Oct 11, 2018 (152)
111	1000Genomes_30x	NC_000001.11 - 177930963	Oct 12, 2022 (156)
112	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 177900098	Oct 11, 2018 (152)
113	Genetic variation in the Estonian population	NC_000001.10 - 177900098	Oct 11, 2018 (152)
114	The Danish reference pan genome	NC_000001.10 - 177900098	Apr 25, 2020 (154)
115	gnomAD - Genomes	NC_000001.11 - 177930963	Apr 25, 2021 (155)
116	Genome of the Netherlands Release 5	NC_000001.10 - 177900098	Apr 25, 2020 (154)
117	HGDP-CEPH-db Supplement 1	NC_000001.9 - 176166721	Apr 25, 2020 (154)
118	HapMap	NC_000001.11 - 177930963	Apr 25, 2020 (154)
119	KOREAN population from KRGDB	NC_000001.10 - 177900098	Apr 25, 2020 (154)
120	Korean Genome Project	NC_000001.11 - 177930963	Apr 25, 2020 (154)
121	Northern Sweden	NC_000001.10 - 177900098	Jul 12, 2019 (153)
122	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000001.10 - 177900098	Apr 25, 2021 (155)
123	Qatari	NC_000001.10 - 177900098	Apr 25, 2020 (154)
124	SGDP_PRJ	NC_000001.10 - 177900098	Apr 25, 2020 (154)
125	Siberian	NC_000001.10 - 177900098	Apr 25, 2020 (154)
126	8.3KJPN	NC_000001.10 - 177900098	Apr 25, 2021 (155)
127	14KJPN	NC_000001.11 - 177930963	Oct 12, 2022 (156)
128	TopMed	NC_000001.11 - 177930963	Apr 25, 2021 (155)
129	UK 10K study - Twins	NC_000001.10 - 177900098	Oct 11, 2018 (152)
130	A Vietnamese Genetic Variation Database	NC_000001.10 - 177900098	Jul 12, 2019 (153)
131	ALFA	NC_000001.11 - 177930963	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)
rs842191	Feb 20, 2003 (111)
rs2152717	Feb 20, 2003 (111)
rs59533866	May 25, 2008 (130)
rs74608969	Aug 21, 2014 (142)
rs200233488	Aug 21, 2014 (142)
rs201318758	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
232170595	NC_000001.11:177930962:T:A	NC_000001.11:177930962:T:A	(self)
ss80753235, ss3638915247, ss3639769594, ss3643822893	NC_000001.8:174631754:T:C	NC_000001.11:177930962:T:C	(self)
32928, ss108728510, ss111393835, ss119106811, ss160746166, ss164504709, ss165480583, ss167312311, ss199287254, ss253629336, ss276114047, ss290670544, ss481157560, ss1585241009, ss1712384420, ss2635004792, ss3642806415, ss3847355036	NC_000001.9:176166720:T:C	NC_000001.11:177930962:T:C	(self)
4387842, 2401651, 1697717, 1774860, 1042913, 2767796, 911382, 62114, 1131325, 2356591, 603986, 5181893, 2401651, 515315, ss218737192, ss230795709, ss238429417, ss481179952, ss482168436, ss485373974, ss537314869, ss554888569, ss648522541, ss778930840, ss783132582, ss784089019, ss832391497, ss833029068, ss833619896, ss834392381, ss975851808, ss1068393312, ss1293573437, ss1426028596, ss1574499827, ss1601561063, ss1644555096, ss1751883575, ss1919089395, ss1966906627, ss2020060144, ss2148087632, ss2624538529, ss2632597484, ss2698068522, ss2763150615, ss2988011959, ss3343786575, ss3626248781, ss3630628969, ss3632916490, ss3633612111, ss3634360096, ss3635305421, ss3636039021, ss3637055931, ss3637798414, ss3640067450, ss3640989083, ss3641283145, ss3655959469, ss3727626517, ss3744660963, ss3747006188, ss3772161992, ss3826507533, ss3836651210, ss3850339611, ss3895590402, ss3984836187, ss5147212586, ss5314663478, ss5506087198, ss5626910921, ss5799504132, ss5832887985, ss5938721382, ss5979296038	NC_000001.10:177900097:T:C	NC_000001.11:177930962:T:C	(self)
5991328, 31721532, 211183, 2348836, 8458712, 37625653, 232170595, ss2167862279, ss3023789311, ss3646826470, ss3688095902, ss3800006315, ss3842061340, ss3945970835, ss4474019318, ss5244852850, ss5445382920, ss5518465393, ss5674621608, ss5801400462, ss5849172700, ss5910889878	NC_000001.11:177930962:T:C	NC_000001.11:177930962:T:C	(self)
ss16399161, ss20570351	NT_004487.16:6948589:T:C	NC_000001.11:177930962:T:C	(self)
ss747335, ss1189664, ss1957233, ss3082276, ss41055886, ss83487736, ss99264822	NT_004487.19:29388739:T:C	NC_000001.11:177930962:T:C	(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 rs575908

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

rs575908