Name: rs573666
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.

rs573666

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr13:50620269 (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: C>T
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.340266 (104050/305790, ALFA)
T=0.299800 (79354/264690, TOPMED)
T=0.306572 (42909/139964, GnomAD) (+ 22 more)
T=0.26051 (20502/78698, PAGE_STUDY)
T=0.14955 (4226/28258, 14KJPN)
T=0.15125 (2535/16760, 8.3KJPN)
T=0.2477 (1586/6404, 1000G_30x)
T=0.2496 (1250/5008, 1000G)
T=0.3346 (1499/4480, Estonian)
T=0.3521 (1357/3854, ALSPAC)
T=0.3557 (1319/3708, TWINSUK)
T=0.2023 (591/2922, KOREAN)
T=0.2442 (509/2084, HGDP_Stanford)
T=0.2329 (437/1876, HapMap)
T=0.2244 (254/1132, Daghestan)
T=0.376 (375/998, GoNL)
T=0.238 (188/790, PRJEB37584)
T=0.291 (182/626, Chileans)
T=0.382 (229/600, NorthernSweden)
C=0.417 (95/228, SGDP_PRJ)
T=0.190 (41/216, Qatari)
T=0.301 (65/216, Vietnamese)
T=0.32 (14/44, Ancient Sardinia)
T=0.28 (11/40, GENOME_DK)
C=0.33 (6/18, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LOC107984567 : Genic Upstream Transcript 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	310824	C=0.660226	T=0.339774
European	Sub	272642	C=0.650120	T=0.349880
African	Sub	9528	C=0.7824	T=0.2176
African Others	Sub	372	C=0.817	T=0.183
African American	Sub	9156	C=0.7810	T=0.2190
Asian	Sub	3944	C=0.7898	T=0.2102
East Asian	Sub	3198	C=0.7880	T=0.2120
Other Asian	Sub	746	C=0.798	T=0.202
Latin American 1	Sub	1168	C=0.7029	T=0.2971
Latin American 2	Sub	8320	C=0.6573	T=0.3427
South Asian	Sub	5224	C=0.7921	T=0.2079
Other	Sub	9998	C=0.6967	T=0.3033

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
Allele Frequency Aggregator	Total	Global	305790	C=0.659734	T=0.340266
Allele Frequency Aggregator	European	Sub	269550	C=0.650173	T=0.349827
Allele Frequency Aggregator	Other	Sub	9198	C=0.6949	T=0.3051
Allele Frequency Aggregator	African	Sub	8386	C=0.7812	T=0.2188
Allele Frequency Aggregator	Latin American 2	Sub	8320	C=0.6573	T=0.3427
Allele Frequency Aggregator	South Asian	Sub	5224	C=0.7921	T=0.2079
Allele Frequency Aggregator	Asian	Sub	3944	C=0.7898	T=0.2102
Allele Frequency Aggregator	Latin American 1	Sub	1168	C=0.7029	T=0.2971
TopMed	Global	Study-wide	264690	C=0.700200	T=0.299800
gnomAD - Genomes	Global	Study-wide	139964	C=0.693428	T=0.306572
gnomAD - Genomes	European	Sub	75802	C=0.64806	T=0.35194
gnomAD - Genomes	African	Sub	41936	C=0.78634	T=0.21366
gnomAD - Genomes	American	Sub	13630	C=0.65598	T=0.34402
gnomAD - Genomes	Ashkenazi Jewish	Sub	3320	C=0.6768	T=0.3232
gnomAD - Genomes	East Asian	Sub	3126	C=0.7380	T=0.2620
gnomAD - Genomes	Other	Sub	2150	C=0.6791	T=0.3209
The PAGE Study	Global	Study-wide	78698	C=0.73949	T=0.26051
The PAGE Study	AfricanAmerican	Sub	32514	C=0.77933	T=0.22067
The PAGE Study	Mexican	Sub	10810	C=0.64903	T=0.35097
The PAGE Study	Asian	Sub	8318	C=0.8268	T=0.1732
The PAGE Study	PuertoRican	Sub	7916	C=0.7244	T=0.2756
The PAGE Study	NativeHawaiian	Sub	4534	C=0.6853	T=0.3147
The PAGE Study	Cuban	Sub	4230	C=0.6574	T=0.3426
The PAGE Study	Dominican	Sub	3828	C=0.7335	T=0.2665
The PAGE Study	CentralAmerican	Sub	2450	C=0.6767	T=0.3233
The PAGE Study	SouthAmerican	Sub	1982	C=0.6892	T=0.3108
The PAGE Study	NativeAmerican	Sub	1260	C=0.6810	T=0.3190
The PAGE Study	SouthAsian	Sub	856	C=0.762	T=0.238
14KJPN	JAPANESE	Study-wide	28258	C=0.85045	T=0.14955
8.3KJPN	JAPANESE	Study-wide	16760	C=0.84875	T=0.15125
1000Genomes_30x	Global	Study-wide	6404	C=0.7523	T=0.2477
1000Genomes_30x	African	Sub	1786	C=0.8214	T=0.1786
1000Genomes_30x	Europe	Sub	1266	C=0.6840	T=0.3160
1000Genomes_30x	South Asian	Sub	1202	C=0.7604	T=0.2396
1000Genomes_30x	East Asian	Sub	1170	C=0.7838	T=0.2162
1000Genomes_30x	American	Sub	980	C=0.667	T=0.333
1000Genomes	Global	Study-wide	5008	C=0.7504	T=0.2496
1000Genomes	African	Sub	1322	C=0.8200	T=0.1800
1000Genomes	East Asian	Sub	1008	C=0.7817	T=0.2183
1000Genomes	Europe	Sub	1006	C=0.6869	T=0.3131
1000Genomes	South Asian	Sub	978	C=0.756	T=0.244
1000Genomes	American	Sub	694	C=0.657	T=0.343
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.6654	T=0.3346
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.6479	T=0.3521
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.6443	T=0.3557
KOREAN population from KRGDB	KOREAN	Study-wide	2922	C=0.7977	T=0.2023
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	C=0.7558	T=0.2442
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	C=0.745	T=0.255
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	C=0.790	T=0.210
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	C=0.746	T=0.254
HGDP-CEPH-db Supplement 1	Europe	Sub	320	C=0.650	T=0.350
HGDP-CEPH-db Supplement 1	Africa	Sub	242	C=0.764	T=0.236
HGDP-CEPH-db Supplement 1	America	Sub	216	C=0.815	T=0.185
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	C=0.94	T=0.06
HapMap	Global	Study-wide	1876	C=0.7671	T=0.2329
HapMap	American	Sub	762	C=0.722	T=0.278
HapMap	African	Sub	686	C=0.809	T=0.191
HapMap	Asian	Sub	254	C=0.831	T=0.169
HapMap	Europe	Sub	174	C=0.707	T=0.293
Genome-wide autozygosity in Daghestan	Global	Study-wide	1132	C=0.7756	T=0.2244
Genome-wide autozygosity in Daghestan	Daghestan	Sub	626	C=0.832	T=0.168
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	C=0.701	T=0.299
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	C=0.779	T=0.221
Genome-wide autozygosity in Daghestan	Europe	Sub	108	C=0.537	T=0.463
Genome-wide autozygosity in Daghestan	South Asian	Sub	96	C=0.81	T=0.19
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	C=0.69	T=0.31
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.624	T=0.376
CNV burdens in cranial meningiomas	Global	Study-wide	790	C=0.762	T=0.238
CNV burdens in cranial meningiomas	CRM	Sub	790	C=0.762	T=0.238
Chileans	Chilean	Study-wide	626	C=0.709	T=0.291
Northern Sweden	ACPOP	Study-wide	600	C=0.618	T=0.382
SGDP_PRJ	Global	Study-wide	228	C=0.417	T=0.583
Qatari	Global	Study-wide	216	C=0.810	T=0.190
A Vietnamese Genetic Variation Database	Global	Study-wide	216	C=0.699	T=0.301
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	44	C=0.68	T=0.32
The Danish reference pan genome	Danish	Study-wide	40	C=0.72	T=0.28
Siberian	Global	Study-wide	18	C=0.33	T=0.67

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 13	NC_000013.11:g.50620269C>T
GRCh37.p13 chr 13	NC_000013.10:g.51194405C>T

Gene: LOC107984567, uncharacterized LOC107984567 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC107984567 transcript variant X6	XR_007063802.1:n.	N/A	Genic Upstream Transcript Variant
LOC107984567 transcript variant X1	XR_007063797.1:n.	N/A	Genic Downstream Transcript Variant
LOC107984567 transcript variant X2	XR_007063798.1:n.	N/A	Genic Downstream Transcript Variant
LOC107984567 transcript variant X3	XR_007063799.1:n.	N/A	Genic Downstream Transcript Variant
LOC107984567 transcript variant X4	XR_007063800.1:n.	N/A	Genic Downstream Transcript Variant
LOC107984567 transcript variant X5	XR_007063801.1:n.	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	C=	T
GRCh38.p14 chr 13	NC_000013.11:g.50620269=	NC_000013.11:g.50620269C>T
GRCh37.p13 chr 13	NC_000013.10:g.51194405=	NC_000013.10:g.51194405C>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#.

142 SubSNP, 25 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SC_JCM	ss745044	Aug 11, 2000 (83)
2	KWOK	ss994432	Oct 04, 2000 (86)
3	KWOK	ss1940664	Oct 18, 2000 (87)
4	KWOK	ss1941207	Oct 18, 2000 (87)
5	SC_JCM	ss2604132	Nov 09, 2000 (92)
6	BCM_SSAHASNP	ss10720416	Jul 11, 2003 (116)
7	CSHL-HAPMAP	ss16618793	Feb 27, 2004 (120)
8	CSHL-HAPMAP	ss17495538	Feb 27, 2004 (120)
9	PERLEGEN	ss24444956	Sep 20, 2004 (123)
10	ABI	ss43546369	Mar 13, 2006 (126)
11	ILLUMINA	ss66653758	Nov 30, 2006 (127)
12	ILLUMINA	ss67419395	Nov 30, 2006 (127)
13	ILLUMINA	ss67780803	Nov 30, 2006 (127)
14	PERLEGEN	ss69134712	May 17, 2007 (127)
15	ILLUMINA	ss70846531	May 23, 2008 (130)
16	ILLUMINA	ss71431210	May 17, 2007 (127)
17	ILLUMINA	ss75516636	Dec 07, 2007 (129)
18	AFFY	ss76574945	Dec 07, 2007 (129)
19	ILLUMINA	ss79209332	Dec 14, 2007 (130)
20	HGSV	ss81497666	Dec 14, 2007 (130)
21	KRIBB_YJKIM	ss83487031	Dec 14, 2007 (130)
22	BCMHGSC_JDW	ss89667934	Mar 24, 2008 (129)
23	HUMANGENOME_JCVI	ss97157669	Feb 02, 2009 (130)
24	1000GENOMES	ss112780583	Jan 25, 2009 (130)
25	1000GENOMES	ss114700499	Jan 25, 2009 (130)
26	ILLUMINA	ss122471744	Dec 01, 2009 (131)
27	ENSEMBL	ss133592919	Dec 01, 2009 (131)
28	ENSEMBL	ss137225186	Dec 01, 2009 (131)
29	ILLUMINA	ss154340350	Dec 01, 2009 (131)
30	GMI	ss154803376	Dec 01, 2009 (131)
31	ILLUMINA	ss159516928	Dec 01, 2009 (131)
32	ILLUMINA	ss160744605	Dec 01, 2009 (131)
33	COMPLETE_GENOMICS	ss169572214	Jul 04, 2010 (132)
34	COMPLETE_GENOMICS	ss171167682	Jul 04, 2010 (132)
35	ILLUMINA	ss172037697	Jul 04, 2010 (132)
36	ILLUMINA	ss173925280	Jul 04, 2010 (132)
37	BCM-HGSC-SUB	ss208624767	Jul 04, 2010 (132)
38	1000GENOMES	ss226187220	Jul 14, 2010 (132)
39	1000GENOMES	ss236253851	Jul 15, 2010 (132)
40	1000GENOMES	ss242749737	Jul 15, 2010 (132)
41	GMI	ss281715384	May 04, 2012 (137)
42	PJP	ss291442170	May 09, 2011 (134)
43	ILLUMINA	ss481153084	May 04, 2012 (137)
44	ILLUMINA	ss481175408	May 04, 2012 (137)
45	ILLUMINA	ss482163790	Sep 08, 2015 (146)
46	ILLUMINA	ss485371727	May 04, 2012 (137)
47	ILLUMINA	ss537313077	Sep 08, 2015 (146)
48	TISHKOFF	ss563669999	Apr 25, 2013 (138)
49	SSMP	ss659274671	Apr 25, 2013 (138)
50	ILLUMINA	ss778930365	Sep 08, 2015 (146)
51	ILLUMINA	ss783131470	Aug 21, 2014 (142)
52	ILLUMINA	ss784087961	Sep 08, 2015 (146)
53	ILLUMINA	ss825539850	Apr 01, 2015 (144)
54	ILLUMINA	ss832390372	Apr 01, 2015 (144)
55	ILLUMINA	ss833028218	Aug 21, 2014 (142)
56	ILLUMINA	ss833619046	Aug 21, 2014 (142)
57	ILLUMINA	ss834391897	Sep 08, 2015 (146)
58	EVA-GONL	ss990394465	Aug 21, 2014 (142)
59	JMKIDD_LAB	ss1079087455	Aug 21, 2014 (142)
60	1000GENOMES	ss1348229025	Aug 21, 2014 (142)
61	HAMMER_LAB	ss1397658358	Sep 08, 2015 (146)
62	DDI	ss1427189304	Apr 01, 2015 (144)
63	EVA_GENOME_DK	ss1576789692	Apr 01, 2015 (144)
64	EVA_UK10K_ALSPAC	ss1630288136	Apr 01, 2015 (144)
65	EVA_UK10K_TWINSUK	ss1673282169	Apr 01, 2015 (144)
66	EVA_DECODE	ss1684918549	Apr 01, 2015 (144)
67	EVA_SVP	ss1713391683	Apr 01, 2015 (144)
68	ILLUMINA	ss1752107267	Sep 08, 2015 (146)
69	HAMMER_LAB	ss1807612228	Sep 08, 2015 (146)
70	WEILL_CORNELL_DGM	ss1933762237	Feb 12, 2016 (147)
71	ILLUMINA	ss1946361249	Feb 12, 2016 (147)
72	ILLUMINA	ss1959501989	Feb 12, 2016 (147)
73	GENOMED	ss1967783726	Jul 19, 2016 (147)
74	JJLAB	ss2027642118	Sep 14, 2016 (149)
75	USC_VALOUEV	ss2156007974	Dec 20, 2016 (150)
76	HUMAN_LONGEVITY	ss2196346424	Dec 20, 2016 (150)
77	ILLUMINA	ss2633064882	Nov 08, 2017 (151)
78	GRF	ss2700387375	Nov 08, 2017 (151)
79	ILLUMINA	ss2710783142	Nov 08, 2017 (151)
80	GNOMAD	ss2919670768	Nov 08, 2017 (151)
81	SWEGEN	ss3011024149	Nov 08, 2017 (151)
82	ILLUMINA	ss3021508945	Nov 08, 2017 (151)
83	BIOINF_KMB_FNS_UNIBA	ss3027637481	Nov 08, 2017 (151)
84	CSHL	ss3350457070	Nov 08, 2017 (151)
85	ILLUMINA	ss3625643818	Oct 12, 2018 (152)
86	ILLUMINA	ss3627066771	Oct 12, 2018 (152)
87	ILLUMINA	ss3631068169	Oct 12, 2018 (152)
88	ILLUMINA	ss3633050462	Oct 12, 2018 (152)
89	ILLUMINA	ss3633752802	Oct 12, 2018 (152)
90	ILLUMINA	ss3634545259	Oct 12, 2018 (152)
91	ILLUMINA	ss3635442881	Oct 12, 2018 (152)
92	ILLUMINA	ss3636232265	Oct 12, 2018 (152)
93	ILLUMINA	ss3637193962	Oct 12, 2018 (152)
94	ILLUMINA	ss3638011807	Oct 12, 2018 (152)
95	ILLUMINA	ss3639018862	Oct 12, 2018 (152)
96	ILLUMINA	ss3639512854	Oct 12, 2018 (152)
97	ILLUMINA	ss3640252589	Oct 12, 2018 (152)
98	ILLUMINA	ss3643001490	Oct 12, 2018 (152)
99	ILLUMINA	ss3644614291	Oct 12, 2018 (152)
100	URBANLAB	ss3650033669	Oct 12, 2018 (152)
101	ILLUMINA	ss3651896618	Oct 12, 2018 (152)
102	EGCUT_WGS	ss3678289614	Jul 13, 2019 (153)
103	EVA_DECODE	ss3695295832	Jul 13, 2019 (153)
104	ILLUMINA	ss3725394778	Jul 13, 2019 (153)
105	ACPOP	ss3739749204	Jul 13, 2019 (153)
106	ILLUMINA	ss3744111801	Jul 13, 2019 (153)
107	ILLUMINA	ss3744845952	Jul 13, 2019 (153)
108	EVA	ss3751466705	Jul 13, 2019 (153)
109	PAGE_CC	ss3771746938	Jul 13, 2019 (153)
110	ILLUMINA	ss3772345018	Jul 13, 2019 (153)
111	PACBIO	ss3787459808	Jul 13, 2019 (153)
112	PACBIO	ss3792525567	Jul 13, 2019 (153)
113	PACBIO	ss3797409394	Jul 13, 2019 (153)
114	KHV_HUMAN_GENOMES	ss3816797006	Jul 13, 2019 (153)
115	EVA	ss3833548038	Apr 27, 2020 (154)
116	EVA	ss3840355508	Apr 27, 2020 (154)
117	EVA	ss3845841351	Apr 27, 2020 (154)
118	HGDP	ss3847479134	Apr 27, 2020 (154)
119	SGDP_PRJ	ss3879979461	Apr 27, 2020 (154)
120	KRGDB	ss3928837042	Apr 27, 2020 (154)
121	EVA	ss3984680486	Apr 26, 2021 (155)
122	EVA	ss3985639937	Apr 26, 2021 (155)
123	EVA	ss4017633601	Apr 26, 2021 (155)
124	TOPMED	ss4946352795	Apr 26, 2021 (155)
125	TOMMO_GENOMICS	ss5210005014	Apr 26, 2021 (155)
126	1000G_HIGH_COVERAGE	ss5293740329	Oct 16, 2022 (156)
127	EVA	ss5315684266	Oct 16, 2022 (156)
128	EVA	ss5410778165	Oct 16, 2022 (156)
129	HUGCELL_USP	ss5488103603	Oct 16, 2022 (156)
130	EVA	ss5510974257	Oct 16, 2022 (156)
131	1000G_HIGH_COVERAGE	ss5592691707	Oct 16, 2022 (156)
132	SANFORD_IMAGENETICS	ss5624324803	Oct 16, 2022 (156)
133	SANFORD_IMAGENETICS	ss5654772938	Oct 16, 2022 (156)
134	TOMMO_GENOMICS	ss5761883404	Oct 16, 2022 (156)
135	EVA	ss5799897828	Oct 16, 2022 (156)
136	YY_MCH	ss5814114161	Oct 16, 2022 (156)
137	EVA	ss5839479923	Oct 16, 2022 (156)
138	EVA	ss5847424633	Oct 16, 2022 (156)
139	EVA	ss5850730834	Oct 16, 2022 (156)
140	EVA	ss5925115131	Oct 16, 2022 (156)
141	EVA	ss5946195713	Oct 16, 2022 (156)
142	EVA	ss5979418897	Oct 16, 2022 (156)
143	1000Genomes	NC_000013.10 - 51194405	Oct 12, 2018 (152)
144	1000Genomes_30x	NC_000013.11 - 50620269	Oct 16, 2022 (156)
145	The Avon Longitudinal Study of Parents and Children	NC_000013.10 - 51194405	Oct 12, 2018 (152)
146	Chileans	NC_000013.10 - 51194405	Apr 27, 2020 (154)
147	Genome-wide autozygosity in Daghestan	NC_000013.9 - 50092406	Apr 27, 2020 (154)
148	Genetic variation in the Estonian population	NC_000013.10 - 51194405	Oct 12, 2018 (152)
149	The Danish reference pan genome	NC_000013.10 - 51194405	Apr 27, 2020 (154)
150	gnomAD - Genomes	NC_000013.11 - 50620269	Apr 26, 2021 (155)
151	Genome of the Netherlands Release 5	NC_000013.10 - 51194405	Apr 27, 2020 (154)
152	HGDP-CEPH-db Supplement 1	NC_000013.9 - 50092406	Apr 27, 2020 (154)
153	HapMap	NC_000013.11 - 50620269	Apr 27, 2020 (154)
154	KOREAN population from KRGDB	NC_000013.10 - 51194405	Apr 27, 2020 (154)
155	Northern Sweden	NC_000013.10 - 51194405	Jul 13, 2019 (153)
156	The PAGE Study	NC_000013.11 - 50620269	Jul 13, 2019 (153)
157	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000013.10 - 51194405	Apr 26, 2021 (155)
158	CNV burdens in cranial meningiomas	NC_000013.10 - 51194405	Apr 26, 2021 (155)
159	Qatari	NC_000013.10 - 51194405	Apr 27, 2020 (154)
160	SGDP_PRJ	NC_000013.10 - 51194405	Apr 27, 2020 (154)
161	Siberian	NC_000013.10 - 51194405	Apr 27, 2020 (154)
162	8.3KJPN	NC_000013.10 - 51194405	Apr 26, 2021 (155)
163	14KJPN	NC_000013.11 - 50620269	Oct 16, 2022 (156)
164	TopMed	NC_000013.11 - 50620269	Apr 26, 2021 (155)
165	UK 10K study - Twins	NC_000013.10 - 51194405	Oct 12, 2018 (152)
166	A Vietnamese Genetic Variation Database	NC_000013.10 - 51194405	Jul 13, 2019 (153)
167	ALFA	NC_000013.11 - 50620269	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)
rs1753653	Jan 18, 2001 (92)
rs17468217	Oct 08, 2004 (123)
rs56696311	May 23, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
128968, 157026, ss76574945, ss81497666, ss89667934, ss112780583, ss114700499, ss169572214, ss171167682, ss208624767, ss281715384, ss291442170, ss481153084, ss825539850, ss1397658358, ss1684918549, ss1713391683, ss3639018862, ss3639512854, ss3643001490, ss3847479134	NC_000013.9:50092405:C:T	NC_000013.11:50620268:C:T	(self)
61100833, 33948563, 120561, 24027862, 3300171, 15146923, 36014436, 13034069, 865864, 229991, 15804167, 31996441, 8524328, 67974321, 33948563, 7532097, ss226187220, ss236253851, ss242749737, ss481175408, ss482163790, ss485371727, ss537313077, ss563669999, ss659274671, ss778930365, ss783131470, ss784087961, ss832390372, ss833028218, ss833619046, ss834391897, ss990394465, ss1079087455, ss1348229025, ss1427189304, ss1576789692, ss1630288136, ss1673282169, ss1752107267, ss1807612228, ss1933762237, ss1946361249, ss1959501989, ss1967783726, ss2027642118, ss2156007974, ss2633064882, ss2700387375, ss2710783142, ss2919670768, ss3011024149, ss3021508945, ss3350457070, ss3625643818, ss3627066771, ss3631068169, ss3633050462, ss3633752802, ss3634545259, ss3635442881, ss3636232265, ss3637193962, ss3638011807, ss3640252589, ss3644614291, ss3651896618, ss3678289614, ss3739749204, ss3744111801, ss3744845952, ss3751466705, ss3772345018, ss3787459808, ss3792525567, ss3797409394, ss3833548038, ss3840355508, ss3879979461, ss3928837042, ss3984680486, ss3985639937, ss4017633601, ss5210005014, ss5315684266, ss5410778165, ss5510974257, ss5624324803, ss5654772938, ss5799897828, ss5839479923, ss5847424633, ss5946195713, ss5979418897	NC_000013.10:51194404:C:T	NC_000013.11:50620268:C:T	(self)
80217642, 430775780, 991704, 968407, 95720508, 161898453, 4204784840, ss2196346424, ss3027637481, ss3650033669, ss3695295832, ss3725394778, ss3771746938, ss3816797006, ss3845841351, ss4946352795, ss5293740329, ss5488103603, ss5592691707, ss5761883404, ss5814114161, ss5850730834, ss5925115131	NC_000013.11:50620268:C:T	NC_000013.11:50620268:C:T	(self)
ss10720416	NT_024524.12:19768896:C:T	NC_000013.11:50620268:C:T	(self)
ss16618793, ss17495538	NT_024524.13:32174405:C:T	NC_000013.11:50620268:C:T	(self)
ss745044, ss994432, ss1940664, ss1941207, ss2604132, ss24444956, ss43546369, ss66653758, ss67419395, ss67780803, ss69134712, ss70846531, ss71431210, ss75516636, ss79209332, ss83487031, ss97157669, ss122471744, ss133592919, ss137225186, ss154340350, ss154803376, ss159516928, ss160744605, ss172037697, ss173925280	NT_024524.14:32174404:C:T	NC_000013.11:50620268:C: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 rs573666

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

rs573666