Name: rs10223700
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.

rs10223700

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:88964142 (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>A
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.161703 (48291/298640, ALFA)
A=0.162806 (43093/264690, TOPMED)
A=0.172652 (24172/140004, GnomAD) (+ 22 more)
A=0.14623 (11506/78684, PAGE_STUDY)
A=0.04038 (1141/28258, 14KJPN)
A=0.04021 (674/16760, 8.3KJPN)
A=0.1604 (1027/6404, 1000G_30x)
A=0.1613 (808/5008, 1000G)
A=0.2165 (970/4480, Estonian)
A=0.1668 (643/3854, ALSPAC)
A=0.1478 (548/3708, TWINSUK)
A=0.0421 (123/2922, KOREAN)
A=0.1099 (229/2084, HGDP_Stanford)
A=0.1485 (280/1886, HapMap)
A=0.0398 (73/1832, Korea1K)
A=0.1508 (171/1134, Daghestan)
A=0.157 (157/998, GoNL)
A=0.059 (46/782, PRJEB37584)
A=0.252 (151/600, NorthernSweden)
A=0.097 (21/216, Qatari)
A=0.033 (7/212, Vietnamese)
C=0.462 (48/104, SGDP_PRJ)
A=0.07 (3/40, GENOME_DK)
A=0.00 (0/26, Ancient Sardinia)
C=0.45 (10/22, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: RNGTT : 2KB Upstream 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	303676	C=0.838239	A=0.161761
European	Sub	268302	C=0.837593	A=0.162407
African	Sub	12126	C=0.79259	A=0.20741
African Others	Sub	454	C=0.811	A=0.189
African American	Sub	11672	C=0.79190	A=0.20810
Asian	Sub	3940	C=0.9627	A=0.0373
East Asian	Sub	3194	C=0.9640	A=0.0360
Other Asian	Sub	746	C=0.957	A=0.043
Latin American 1	Sub	1074	C=0.8613	A=0.1387
Latin American 2	Sub	3160	C=0.9054	A=0.0946
South Asian	Sub	5204	C=0.8000	A=0.2000
Other	Sub	9870	C=0.8584	A=0.1416

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	298640	C=0.838297	A=0.161703
Allele Frequency Aggregator	European	Sub	265208	C=0.837512	A=0.162488
Allele Frequency Aggregator	African	Sub	10984	C=0.79261	A=0.20739
Allele Frequency Aggregator	Other	Sub	9070	C=0.8584	A=0.1416
Allele Frequency Aggregator	South Asian	Sub	5204	C=0.8000	A=0.2000
Allele Frequency Aggregator	Asian	Sub	3940	C=0.9627	A=0.0373
Allele Frequency Aggregator	Latin American 2	Sub	3160	C=0.9054	A=0.0946
Allele Frequency Aggregator	Latin American 1	Sub	1074	C=0.8613	A=0.1387
TopMed	Global	Study-wide	264690	C=0.837194	A=0.162806
gnomAD - Genomes	Global	Study-wide	140004	C=0.827348	A=0.172652
gnomAD - Genomes	European	Sub	75830	C=0.83244	A=0.16756
gnomAD - Genomes	African	Sub	41942	C=0.79345	A=0.20655
gnomAD - Genomes	American	Sub	13636	C=0.88120	A=0.11880
gnomAD - Genomes	Ashkenazi Jewish	Sub	3320	C=0.8066	A=0.1934
gnomAD - Genomes	East Asian	Sub	3124	C=0.9389	A=0.0611
gnomAD - Genomes	Other	Sub	2152	C=0.8374	A=0.1626
The PAGE Study	Global	Study-wide	78684	C=0.85377	A=0.14623
The PAGE Study	AfricanAmerican	Sub	32502	C=0.79435	A=0.20565
The PAGE Study	Mexican	Sub	10810	C=0.91767	A=0.08233
The PAGE Study	Asian	Sub	8318	C=0.9566	A=0.0434
The PAGE Study	PuertoRican	Sub	7918	C=0.8579	A=0.1421
The PAGE Study	NativeHawaiian	Sub	4534	C=0.9411	A=0.0589
The PAGE Study	Cuban	Sub	4230	C=0.8243	A=0.1757
The PAGE Study	Dominican	Sub	3828	C=0.8252	A=0.1748
The PAGE Study	CentralAmerican	Sub	2450	C=0.8992	A=0.1008
The PAGE Study	SouthAmerican	Sub	1982	C=0.9062	A=0.0938
The PAGE Study	NativeAmerican	Sub	1260	C=0.8595	A=0.1405
The PAGE Study	SouthAsian	Sub	852	C=0.816	A=0.184
14KJPN	JAPANESE	Study-wide	28258	C=0.95962	A=0.04038
8.3KJPN	JAPANESE	Study-wide	16760	C=0.95979	A=0.04021
1000Genomes_30x	Global	Study-wide	6404	C=0.8396	A=0.1604
1000Genomes_30x	African	Sub	1786	C=0.7699	A=0.2301
1000Genomes_30x	Europe	Sub	1266	C=0.8460	A=0.1540
1000Genomes_30x	South Asian	Sub	1202	C=0.7845	A=0.2155
1000Genomes_30x	East Asian	Sub	1170	C=0.9385	A=0.0615
1000Genomes_30x	American	Sub	980	C=0.908	A=0.092
1000Genomes	Global	Study-wide	5008	C=0.8387	A=0.1613
1000Genomes	African	Sub	1322	C=0.7655	A=0.2345
1000Genomes	East Asian	Sub	1008	C=0.9415	A=0.0585
1000Genomes	Europe	Sub	1006	C=0.8449	A=0.1551
1000Genomes	South Asian	Sub	978	C=0.781	A=0.219
1000Genomes	American	Sub	694	C=0.901	A=0.099
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.7835	A=0.2165
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.8332	A=0.1668
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.8522	A=0.1478
KOREAN population from KRGDB	KOREAN	Study-wide	2922	C=0.9579	A=0.0421
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	C=0.8901	A=0.1099
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	C=0.945	A=0.055
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	C=0.862	A=0.138
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	C=0.837	A=0.163
HGDP-CEPH-db Supplement 1	Europe	Sub	320	C=0.850	A=0.150
HGDP-CEPH-db Supplement 1	Africa	Sub	242	C=0.847	A=0.153
HGDP-CEPH-db Supplement 1	America	Sub	216	C=0.981	A=0.019
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	C=1.00	A=0.00
HapMap	Global	Study-wide	1886	C=0.8515	A=0.1485
HapMap	American	Sub	768	C=0.858	A=0.142
HapMap	African	Sub	688	C=0.788	A=0.212
HapMap	Asian	Sub	254	C=0.965	A=0.035
HapMap	Europe	Sub	176	C=0.909	A=0.091
Korean Genome Project	KOREAN	Study-wide	1832	C=0.9602	A=0.0398
Genome-wide autozygosity in Daghestan	Global	Study-wide	1134	C=0.8492	A=0.1508
Genome-wide autozygosity in Daghestan	Daghestan	Sub	628	C=0.850	A=0.150
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	C=0.819	A=0.181
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	C=0.910	A=0.090
Genome-wide autozygosity in Daghestan	Europe	Sub	108	C=0.806	A=0.194
Genome-wide autozygosity in Daghestan	South Asian	Sub	96	C=0.82	A=0.18
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	C=0.94	A=0.06
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.843	A=0.157
CNV burdens in cranial meningiomas	Global	Study-wide	782	C=0.941	A=0.059
CNV burdens in cranial meningiomas	CRM	Sub	782	C=0.941	A=0.059
Northern Sweden	ACPOP	Study-wide	600	C=0.748	A=0.252
Qatari	Global	Study-wide	216	C=0.903	A=0.097
A Vietnamese Genetic Variation Database	Global	Study-wide	212	C=0.967	A=0.033
SGDP_PRJ	Global	Study-wide	104	C=0.462	A=0.538
The Danish reference pan genome	Danish	Study-wide	40	C=0.93	A=0.07
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	26	C=1.00	A=0.00
Siberian	Global	Study-wide	22	C=0.45	A=0.55

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 6	NC_000006.12:g.88964142C>A
GRCh37.p13 chr 6	NC_000006.11:g.89673861C>A

Gene: RNGTT, RNA guanylyltransferase and 5'-phosphatase (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
RNGTT transcript variant 2	NM_001286426.2:c.	N/A	Upstream Transcript Variant
RNGTT transcript variant 3	NM_001286428.2:c.	N/A	Upstream Transcript Variant
RNGTT transcript variant 1	NM_003800.5:c.	N/A	Upstream Transcript Variant
RNGTT transcript variant X1	XM_047419442.1:c.	N/A	Upstream Transcript Variant
RNGTT transcript variant X2	XM_047419443.1:c.	N/A	Upstream 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=	A
GRCh38.p14 chr 6	NC_000006.12:g.88964142=	NC_000006.12:g.88964142C>A
GRCh37.p13 chr 6	NC_000006.11:g.89673861=	NC_000006.11:g.89673861C>A

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#.

122 SubSNP, 25 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	WUGSC_SSAHASNP	ss14093267	Dec 05, 2003 (119)
2	CSHL-HAPMAP	ss17899650	Feb 27, 2004 (120)
3	KYUGEN	ss28460206	Sep 20, 2004 (123)
4	ILLUMINA	ss66793208	Nov 29, 2006 (127)
5	ILLUMINA	ss66876914	Nov 29, 2006 (127)
6	ILLUMINA	ss66961805	Nov 29, 2006 (127)
7	ILLUMINA	ss70362313	May 16, 2007 (127)
8	ILLUMINA	ss70472532	May 23, 2008 (130)
9	ILLUMINA	ss70994502	May 16, 2007 (127)
10	ILLUMINA	ss75863537	Dec 07, 2007 (129)
11	KRIBB_YJKIM	ss84924715	Dec 14, 2007 (130)
12	1000GENOMES	ss110505894	Jan 24, 2009 (130)
13	ILLUMINA	ss121285660	Dec 01, 2009 (131)
14	ILLUMINA	ss152608075	Dec 01, 2009 (131)
15	ILLUMINA	ss159116784	Dec 01, 2009 (131)
16	ILLUMINA	ss159879841	Dec 01, 2009 (131)
17	COMPLETE_GENOMICS	ss166995448	Jul 04, 2010 (132)
18	ILLUMINA	ss169323835	Jul 04, 2010 (132)
19	ILLUMINA	ss169879632	Jul 04, 2010 (132)
20	BUSHMAN	ss202154317	Jul 04, 2010 (132)
21	1000GENOMES	ss211882180	Jul 14, 2010 (132)
22	1000GENOMES	ss222529688	Jul 14, 2010 (132)
23	1000GENOMES	ss233577619	Jul 15, 2010 (132)
24	BL	ss254538776	May 09, 2011 (134)
25	ILLUMINA	ss479229309	May 04, 2012 (137)
26	ILLUMINA	ss479231800	May 04, 2012 (137)
27	ILLUMINA	ss479585426	Sep 08, 2015 (146)
28	ILLUMINA	ss484415429	May 04, 2012 (137)
29	ILLUMINA	ss536591544	Sep 08, 2015 (146)
30	TISHKOFF	ss559359866	Apr 25, 2013 (138)
31	SSMP	ss653355078	Apr 25, 2013 (138)
32	ILLUMINA	ss778351850	Sep 08, 2015 (146)
33	ILLUMINA	ss782654149	Sep 08, 2015 (146)
34	ILLUMINA	ss783623315	Sep 08, 2015 (146)
35	ILLUMINA	ss825332044	Apr 01, 2015 (144)
36	ILLUMINA	ss831904526	Sep 08, 2015 (146)
37	ILLUMINA	ss832629524	Jul 13, 2019 (153)
38	ILLUMINA	ss833806550	Sep 08, 2015 (146)
39	EVA-GONL	ss983213009	Aug 21, 2014 (142)
40	JMKIDD_LAB	ss1073817922	Aug 21, 2014 (142)
41	1000GENOMES	ss1321190340	Aug 21, 2014 (142)
42	HAMMER_LAB	ss1397462757	Sep 08, 2015 (146)
43	DDI	ss1430814345	Apr 01, 2015 (144)
44	EVA_GENOME_DK	ss1581784675	Apr 01, 2015 (144)
45	EVA_DECODE	ss1592765375	Apr 01, 2015 (144)
46	EVA_UK10K_ALSPAC	ss1616115908	Apr 01, 2015 (144)
47	EVA_UK10K_TWINSUK	ss1659109941	Apr 01, 2015 (144)
48	EVA_SVP	ss1712880361	Apr 01, 2015 (144)
49	ILLUMINA	ss1752651559	Sep 08, 2015 (146)
50	HAMMER_LAB	ss1804551596	Sep 08, 2015 (146)
51	WEILL_CORNELL_DGM	ss1926470525	Feb 12, 2016 (147)
52	ILLUMINA	ss1946185203	Feb 12, 2016 (147)
53	ILLUMINA	ss1958931247	Feb 12, 2016 (147)
54	JJLAB	ss2023878480	Sep 14, 2016 (149)
55	USC_VALOUEV	ss2152070444	Dec 20, 2016 (150)
56	HUMAN_LONGEVITY	ss2286063252	Dec 20, 2016 (150)
57	SYSTEMSBIOZJU	ss2626434061	Nov 08, 2017 (151)
58	ILLUMINA	ss2634479959	Nov 08, 2017 (151)
59	GRF	ss2707689420	Nov 08, 2017 (151)
60	ILLUMINA	ss2711083853	Nov 08, 2017 (151)
61	GNOMAD	ss2841987625	Nov 08, 2017 (151)
62	SWEGEN	ss2999513292	Nov 08, 2017 (151)
63	ILLUMINA	ss3022644130	Nov 08, 2017 (151)
64	BIOINF_KMB_FNS_UNIBA	ss3025733119	Nov 08, 2017 (151)
65	CSHL	ss3347104000	Nov 08, 2017 (151)
66	ILLUMINA	ss3625907199	Oct 12, 2018 (152)
67	ILLUMINA	ss3629598485	Oct 12, 2018 (152)
68	ILLUMINA	ss3632394910	Oct 12, 2018 (152)
69	ILLUMINA	ss3633429217	Oct 12, 2018 (152)
70	ILLUMINA	ss3634152447	Oct 12, 2018 (152)
71	ILLUMINA	ss3635077457	Oct 12, 2018 (152)
72	ILLUMINA	ss3635833105	Oct 12, 2018 (152)
73	ILLUMINA	ss3636801391	Oct 12, 2018 (152)
74	ILLUMINA	ss3637585937	Oct 12, 2018 (152)
75	ILLUMINA	ss3638643035	Oct 12, 2018 (152)
76	ILLUMINA	ss3639322056	Oct 12, 2018 (152)
77	ILLUMINA	ss3639687380	Oct 12, 2018 (152)
78	ILLUMINA	ss3640784758	Oct 12, 2018 (152)
79	ILLUMINA	ss3643583166	Oct 12, 2018 (152)
80	ILLUMINA	ss3644918284	Oct 12, 2018 (152)
81	ILLUMINA	ss3653161886	Oct 12, 2018 (152)
82	EGCUT_WGS	ss3667394733	Jul 13, 2019 (153)
83	EVA_DECODE	ss3717734680	Jul 13, 2019 (153)
84	ILLUMINA	ss3726363935	Jul 13, 2019 (153)
85	ACPOP	ss3733742917	Jul 13, 2019 (153)
86	ILLUMINA	ss3744274913	Jul 13, 2019 (153)
87	ILLUMINA	ss3745377398	Jul 13, 2019 (153)
88	EVA	ss3765338615	Jul 13, 2019 (153)
89	PAGE_CC	ss3771307300	Jul 13, 2019 (153)
90	ILLUMINA	ss3772870872	Jul 13, 2019 (153)
91	KHV_HUMAN_GENOMES	ss3808489683	Jul 13, 2019 (153)
92	EVA	ss3830061052	Apr 26, 2020 (154)
93	EVA	ss3838511853	Apr 26, 2020 (154)
94	EVA	ss3843959821	Apr 26, 2020 (154)
95	HGDP	ss3847841671	Apr 26, 2020 (154)
96	SGDP_PRJ	ss3865139523	Apr 26, 2020 (154)
97	KRGDB	ss3912033702	Apr 26, 2020 (154)
98	KOGIC	ss3959552012	Apr 26, 2020 (154)
99	EVA	ss3984572622	Apr 26, 2021 (155)
100	EVA	ss3985236283	Apr 26, 2021 (155)
101	EVA	ss4017286686	Apr 26, 2021 (155)
102	TOPMED	ss4712211931	Apr 26, 2021 (155)
103	TOMMO_GENOMICS	ss5178697955	Apr 26, 2021 (155)
104	EVA	ss5237402553	Apr 26, 2021 (155)
105	1000G_HIGH_COVERAGE	ss5269387915	Oct 14, 2022 (156)
106	EVA	ss5315172170	Oct 14, 2022 (156)
107	EVA	ss5367278428	Oct 14, 2022 (156)
108	HUGCELL_USP	ss5466922663	Oct 14, 2022 (156)
109	EVA	ss5508608769	Oct 14, 2022 (156)
110	1000G_HIGH_COVERAGE	ss5555810710	Oct 14, 2022 (156)
111	SANFORD_IMAGENETICS	ss5624635458	Oct 14, 2022 (156)
112	SANFORD_IMAGENETICS	ss5640944816	Oct 14, 2022 (156)
113	TOMMO_GENOMICS	ss5717221426	Oct 14, 2022 (156)
114	EVA	ss5799695203	Oct 14, 2022 (156)
115	YY_MCH	ss5807716500	Oct 14, 2022 (156)
116	EVA	ss5842620138	Oct 14, 2022 (156)
117	EVA	ss5847299014	Oct 14, 2022 (156)
118	EVA	ss5848105062	Oct 14, 2022 (156)
119	EVA	ss5855465408	Oct 14, 2022 (156)
120	EVA	ss5884854991	Oct 14, 2022 (156)
121	EVA	ss5969448448	Oct 14, 2022 (156)
122	EVA	ss5979794292	Oct 14, 2022 (156)
123	1000Genomes	NC_000006.11 - 89673861	Oct 12, 2018 (152)
124	1000Genomes_30x	NC_000006.12 - 88964142	Oct 14, 2022 (156)
125	The Avon Longitudinal Study of Parents and Children	NC_000006.11 - 89673861	Oct 12, 2018 (152)
126	Genome-wide autozygosity in Daghestan	NC_000006.10 - 89730580	Apr 26, 2020 (154)
127	Genetic variation in the Estonian population	NC_000006.11 - 89673861	Oct 12, 2018 (152)
128	The Danish reference pan genome	NC_000006.11 - 89673861	Apr 26, 2020 (154)
129	gnomAD - Genomes	NC_000006.12 - 88964142	Apr 26, 2021 (155)
130	Genome of the Netherlands Release 5	NC_000006.11 - 89673861	Apr 26, 2020 (154)
131	HGDP-CEPH-db Supplement 1	NC_000006.10 - 89730580	Apr 26, 2020 (154)
132	HapMap	NC_000006.12 - 88964142	Apr 26, 2020 (154)
133	KOREAN population from KRGDB	NC_000006.11 - 89673861	Apr 26, 2020 (154)
134	Korean Genome Project	NC_000006.12 - 88964142	Apr 26, 2020 (154)
135	Northern Sweden	NC_000006.11 - 89673861	Jul 13, 2019 (153)
136	The PAGE Study	NC_000006.12 - 88964142	Jul 13, 2019 (153)
137	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000006.11 - 89673861	Apr 26, 2021 (155)
138	CNV burdens in cranial meningiomas	NC_000006.11 - 89673861	Apr 26, 2021 (155)
139	Qatari	NC_000006.11 - 89673861	Apr 26, 2020 (154)
140	SGDP_PRJ	NC_000006.11 - 89673861	Apr 26, 2020 (154)
141	Siberian	NC_000006.11 - 89673861	Apr 26, 2020 (154)
142	8.3KJPN	NC_000006.11 - 89673861	Apr 26, 2021 (155)
143	14KJPN	NC_000006.12 - 88964142	Oct 14, 2022 (156)
144	TopMed	NC_000006.12 - 88964142	Apr 26, 2021 (155)
145	UK 10K study - Twins	NC_000006.11 - 89673861	Oct 12, 2018 (152)
146	A Vietnamese Genetic Variation Database	NC_000006.11 - 89673861	Jul 13, 2019 (153)
147	ALFA	NC_000006.12 - 88964142	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)
rs57286506	May 23, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3639322056, ss3639687380	NC_000006.9:89730579:C:A	NC_000006.12:88964141:C:A	(self)
437277, 519563, ss110505894, ss166995448, ss202154317, ss211882180, ss254538776, ss479229309, ss825332044, ss1397462757, ss1592765375, ss1712880361, ss3643583166, ss3847841671	NC_000006.10:89730579:C:A	NC_000006.12:88964141:C:A	(self)
33017547, 18388876, 13132981, 7949614, 8194595, 19211096, 7027782, 462210, 122032, 8512455, 17156503, 4586798, 36667262, 18388876, 4087477, ss222529688, ss233577619, ss479231800, ss479585426, ss484415429, ss536591544, ss559359866, ss653355078, ss778351850, ss782654149, ss783623315, ss831904526, ss832629524, ss833806550, ss983213009, ss1073817922, ss1321190340, ss1430814345, ss1581784675, ss1616115908, ss1659109941, ss1752651559, ss1804551596, ss1926470525, ss1946185203, ss1958931247, ss2023878480, ss2152070444, ss2626434061, ss2634479959, ss2707689420, ss2711083853, ss2841987625, ss2999513292, ss3022644130, ss3347104000, ss3625907199, ss3629598485, ss3632394910, ss3633429217, ss3634152447, ss3635077457, ss3635833105, ss3636801391, ss3637585937, ss3638643035, ss3640784758, ss3644918284, ss3653161886, ss3667394733, ss3733742917, ss3744274913, ss3745377398, ss3765338615, ss3772870872, ss3830061052, ss3838511853, ss3865139523, ss3912033702, ss3984572622, ss3985236283, ss4017286686, ss5178697955, ss5237402553, ss5315172170, ss5367278428, ss5508608769, ss5624635458, ss5640944816, ss5799695203, ss5842620138, ss5847299014, ss5848105062, ss5969448448, ss5979794292	NC_000006.11:89673860:C:A	NC_000006.12:88964141:C:A	(self)
43336645, 232998212, 3187597, 15930013, 528769, 51058530, 549589489, 2270072944, ss2286063252, ss3025733119, ss3717734680, ss3726363935, ss3771307300, ss3808489683, ss3843959821, ss3959552012, ss4712211931, ss5269387915, ss5466922663, ss5555810710, ss5717221426, ss5807716500, ss5855465408, ss5884854991	NC_000006.12:88964141:C:A	NC_000006.12:88964141:C:A	(self)
ss14093267, ss17899650	NT_007299.12:27494031:C:A	NC_000006.12:88964141:C:A	(self)
ss28460206, ss66793208, ss66876914, ss66961805, ss70362313, ss70472532, ss70994502, ss75863537, ss84924715, ss121285660, ss152608075, ss159116784, ss159879841, ss169323835, ss169879632	NT_007299.13:27793694:C:A	NC_000006.12:88964141:C:A	(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 rs10223700

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.
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

rs10223700