Name: rs6835141
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.

rs6835141

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:1076352 (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>A / G>C / G>T
Variation Type: SNV Single Nucleotide Variation
Frequency: G=0.212581 (56268/264690, TOPMED)
G=0.199752 (28000/140174, GnomAD)
G=0.46001 (12999/28258, 14KJPN) (+ 15 more)
G=0.22262 (5772/25928, ALFA)
G=0.45800 (7676/16760, 8.3KJPN)
G=0.2392 (1532/6404, 1000G_30x)
G=0.2426 (1215/5008, 1000G)
G=0.1484 (665/4480, Estonian)
G=0.2309 (890/3854, ALSPAC)
G=0.2257 (837/3708, TWINSUK)
G=0.4406 (1291/2930, KOREAN)
G=0.205 (205/998, GoNL)
G=0.245 (147/600, NorthernSweden)
G=0.203 (101/498, SGDP_PRJ)
G=0.269 (58/216, Qatari)
G=0.382 (81/212, Vietnamese)
G=0.21 (11/52, Siberian)
G=0.23 (9/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: RNF212 : 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	25928	G=0.22262	T=0.77738
European	Sub	14646	G=0.19842	T=0.80158
African	Sub	3248	G=0.1192	T=0.8808
African Others	Sub	114	G=0.079	T=0.921
African American	Sub	3134	G=0.1206	T=0.8794
Asian	Sub	134	G=0.455	T=0.545
East Asian	Sub	104	G=0.442	T=0.558
Other Asian	Sub	30	G=0.50	T=0.50
Latin American 1	Sub	222	G=0.212	T=0.788
Latin American 2	Sub	4540	G=0.3709	T=0.6291
South Asian	Sub	114	G=0.246	T=0.754
Other	Sub	3024	G=0.2179	T=0.7821

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=0.212581	T=0.787419
gnomAD - Genomes	Global	Study-wide	140174	G=0.199752	T=0.800248
gnomAD - Genomes	European	Sub	75908	G=0.21393	T=0.78607
gnomAD - Genomes	African	Sub	42020	G=0.11713	T=0.88287
gnomAD - Genomes	American	Sub	13654	G=0.32635	T=0.67365
gnomAD - Genomes	Ashkenazi Jewish	Sub	3320	G=0.2169	T=0.7831
gnomAD - Genomes	East Asian	Sub	3122	G=0.3776	T=0.6224
gnomAD - Genomes	Other	Sub	2150	G=0.2251	T=0.7749
14KJPN	JAPANESE	Study-wide	28258	G=0.46001	T=0.53999
Allele Frequency Aggregator	Total	Global	25928	G=0.22262	T=0.77738
Allele Frequency Aggregator	European	Sub	14646	G=0.19842	T=0.80158
Allele Frequency Aggregator	Latin American 2	Sub	4540	G=0.3709	T=0.6291
Allele Frequency Aggregator	African	Sub	3248	G=0.1192	T=0.8808
Allele Frequency Aggregator	Other	Sub	3024	G=0.2179	T=0.7821
Allele Frequency Aggregator	Latin American 1	Sub	222	G=0.212	T=0.788
Allele Frequency Aggregator	Asian	Sub	134	G=0.455	T=0.545
Allele Frequency Aggregator	South Asian	Sub	114	G=0.246	T=0.754
8.3KJPN	JAPANESE	Study-wide	16760	G=0.45800	T=0.54200
1000Genomes_30x	Global	Study-wide	6404	G=0.2392	T=0.7608
1000Genomes_30x	African	Sub	1786	G=0.0862	T=0.9138
1000Genomes_30x	Europe	Sub	1266	G=0.2591	T=0.7409
1000Genomes_30x	South Asian	Sub	1202	G=0.2529	T=0.7471
1000Genomes_30x	East Asian	Sub	1170	G=0.3444	T=0.6556
1000Genomes_30x	American	Sub	980	G=0.350	T=0.650
1000Genomes	Global	Study-wide	5008	G=0.2426	T=0.7574
1000Genomes	African	Sub	1322	G=0.0923	T=0.9077
1000Genomes	East Asian	Sub	1008	G=0.3502	T=0.6498
1000Genomes	Europe	Sub	1006	G=0.2445	T=0.7555
1000Genomes	South Asian	Sub	978	G=0.252	T=0.748
1000Genomes	American	Sub	694	G=0.357	T=0.643
Genetic variation in the Estonian population	Estonian	Study-wide	4480	G=0.1484	T=0.8516
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.2309	T=0.7691
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.2257	T=0.7743
KOREAN population from KRGDB	KOREAN	Study-wide	2930	G=0.4406	A=0.0003, C=0.0000, T=0.5590
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	G=0.205	T=0.795
Northern Sweden	ACPOP	Study-wide	600	G=0.245	T=0.755
SGDP_PRJ	Global	Study-wide	498	G=0.203	T=0.797
Qatari	Global	Study-wide	216	G=0.269	T=0.731
A Vietnamese Genetic Variation Database	Global	Study-wide	212	G=0.382	T=0.618
Siberian	Global	Study-wide	52	G=0.21	T=0.79
The Danish reference pan genome	Danish	Study-wide	40	G=0.23	T=0.78

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 4	NC_000004.12:g.1076352G>A
GRCh38.p14 chr 4	NC_000004.12:g.1076352G>C
GRCh38.p14 chr 4	NC_000004.12:g.1076352G>T
GRCh37.p13 chr 4	NC_000004.11:g.1070140G>A
GRCh37.p13 chr 4	NC_000004.11:g.1070140G>C
GRCh37.p13 chr 4	NC_000004.11:g.1070140G>T
RNF212 RefSeqGene	NG_027812.2:g.42443C>T
RNF212 RefSeqGene	NG_027812.2:g.42443C>G
RNF212 RefSeqGene	NG_027812.2:g.42443C>A

Gene: RNF212, ring finger protein 212 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
RNF212 transcript variant 1	NM_001131034.4:c.511-2690… NM_001131034.4:c.511-2690C>T	N/A	Intron Variant
RNF212 transcript variant 4	NM_001366918.1:c.511-2690… NM_001366918.1:c.511-2690C>T	N/A	Intron Variant
RNF212 transcript variant 5	NM_001366919.1:c.511-2690… NM_001366919.1:c.511-2690C>T	N/A	Intron Variant
RNF212 transcript variant 2	NM_194439.5:c.511-2690C>T	N/A	Intron Variant
RNF212 transcript variant 3	NM_001193318.3:c.	N/A	Genic Downstream Transcript Variant
RNF212 transcript variant 6	NR_159497.1:n.	N/A	Intron Variant
RNF212 transcript variant 7	NR_159498.1:n.	N/A	Intron Variant
RNF212 transcript variant 8	NR_159499.1:n.	N/A	Intron Variant
RNF212 transcript variant 9	NR_159500.1:n.	N/A	Intron Variant
RNF212 transcript variant 10	NR_159501.1:n.	N/A	Intron Variant
RNF212 transcript variant 11	NR_159502.1:n.	N/A	Intron Variant
RNF212 transcript variant 12	NR_159503.1:n.	N/A	Intron Variant
RNF212 transcript variant 13	NR_159504.1:n.	N/A	Intron Variant
RNF212 transcript variant 14	NR_159505.1:n.	N/A	Intron Variant
RNF212 transcript variant X2	XM_011513439.2:c.379-2690… XM_011513439.2:c.379-2690C>T	N/A	Intron Variant
RNF212 transcript variant X7	XM_011513445.3:c.247-2690… XM_011513445.3:c.247-2690C>T	N/A	Intron Variant
RNF212 transcript variant X10	XM_011513446.2:c.247-2690… XM_011513446.2:c.247-2690C>T	N/A	Intron Variant
RNF212 transcript variant X3	XM_017008040.2:c.379-2690… XM_017008040.2:c.379-2690C>T	N/A	Intron Variant
RNF212 transcript variant X1	XM_047450082.1:c.511-2690… XM_047450082.1:c.511-2690C>T	N/A	Intron Variant
RNF212 transcript variant X4	XM_047450083.1:c.409-2690… XM_047450083.1:c.409-2690C>T	N/A	Intron Variant
RNF212 transcript variant X5	XM_047450084.1:c.511-2690… XM_047450084.1:c.511-2690C>T	N/A	Intron Variant
RNF212 transcript variant X6	XM_047450085.1:c.313-2690… XM_047450085.1:c.313-2690C>T	N/A	Intron Variant
RNF212 transcript variant X8	XM_047450086.1:c.409-2690… XM_047450086.1:c.409-2690C>T	N/A	Intron Variant
RNF212 transcript variant X9	XM_047450087.1:c.379-2690… XM_047450087.1:c.379-2690C>T	N/A	Intron Variant
RNF212 transcript variant X11	XM_047450088.1:c.343-2690… XM_047450088.1:c.343-2690C>T	N/A	Intron Variant
RNF212 transcript variant X12	XM_017008041.2:c.	N/A	Genic Downstream Transcript Variant
RNF212 transcript variant X14	XR_007096392.1:n.	N/A	Intron Variant
RNF212 transcript variant X13	XR_924937.2:n.	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=	A	C	T
GRCh38.p14 chr 4	NC_000004.12:g.1076352=	NC_000004.12:g.1076352G>A	NC_000004.12:g.1076352G>C	NC_000004.12:g.1076352G>T
GRCh37.p13 chr 4	NC_000004.11:g.1070140=	NC_000004.11:g.1070140G>A	NC_000004.11:g.1070140G>C	NC_000004.11:g.1070140G>T
RNF212 RefSeqGene	NG_027812.2:g.42443=	NG_027812.2:g.42443C>T	NG_027812.2:g.42443C>G	NG_027812.2:g.42443C>A
RNF212 transcript variant 1	NM_001131034.3:c.511-2690=	NM_001131034.3:c.511-2690C>T	NM_001131034.3:c.511-2690C>G	NM_001131034.3:c.511-2690C>A
RNF212 transcript variant 1	NM_001131034.4:c.511-2690=	NM_001131034.4:c.511-2690C>T	NM_001131034.4:c.511-2690C>G	NM_001131034.4:c.511-2690C>A
RNF212 transcript variant 4	NM_001366918.1:c.511-2690=	NM_001366918.1:c.511-2690C>T	NM_001366918.1:c.511-2690C>G	NM_001366918.1:c.511-2690C>A
RNF212 transcript variant 5	NM_001366919.1:c.511-2690=	NM_001366919.1:c.511-2690C>T	NM_001366919.1:c.511-2690C>G	NM_001366919.1:c.511-2690C>A
RNF212 transcript variant 2	NM_194439.4:c.511-2690=	NM_194439.4:c.511-2690C>T	NM_194439.4:c.511-2690C>G	NM_194439.4:c.511-2690C>A
RNF212 transcript variant 2	NM_194439.5:c.511-2690=	NM_194439.5:c.511-2690C>T	NM_194439.5:c.511-2690C>G	NM_194439.5:c.511-2690C>A
RNF212 transcript variant X1	XM_005272274.1:c.511-2690=	XM_005272274.1:c.511-2690C>T	XM_005272274.1:c.511-2690C>G	XM_005272274.1:c.511-2690C>A
RNF212 transcript variant X2	XM_005272275.1:c.511-2690=	XM_005272275.1:c.511-2690C>T	XM_005272275.1:c.511-2690C>G	XM_005272275.1:c.511-2690C>A
RNF212 transcript variant X2	XM_011513439.2:c.379-2690=	XM_011513439.2:c.379-2690C>T	XM_011513439.2:c.379-2690C>G	XM_011513439.2:c.379-2690C>A
RNF212 transcript variant X7	XM_011513445.3:c.247-2690=	XM_011513445.3:c.247-2690C>T	XM_011513445.3:c.247-2690C>G	XM_011513445.3:c.247-2690C>A
RNF212 transcript variant X10	XM_011513446.2:c.247-2690=	XM_011513446.2:c.247-2690C>T	XM_011513446.2:c.247-2690C>G	XM_011513446.2:c.247-2690C>A
RNF212 transcript variant X3	XM_017008040.2:c.379-2690=	XM_017008040.2:c.379-2690C>T	XM_017008040.2:c.379-2690C>G	XM_017008040.2:c.379-2690C>A
RNF212 transcript variant X1	XM_047450082.1:c.511-2690=	XM_047450082.1:c.511-2690C>T	XM_047450082.1:c.511-2690C>G	XM_047450082.1:c.511-2690C>A
RNF212 transcript variant X4	XM_047450083.1:c.409-2690=	XM_047450083.1:c.409-2690C>T	XM_047450083.1:c.409-2690C>G	XM_047450083.1:c.409-2690C>A
RNF212 transcript variant X5	XM_047450084.1:c.511-2690=	XM_047450084.1:c.511-2690C>T	XM_047450084.1:c.511-2690C>G	XM_047450084.1:c.511-2690C>A
RNF212 transcript variant X6	XM_047450085.1:c.313-2690=	XM_047450085.1:c.313-2690C>T	XM_047450085.1:c.313-2690C>G	XM_047450085.1:c.313-2690C>A
RNF212 transcript variant X8	XM_047450086.1:c.409-2690=	XM_047450086.1:c.409-2690C>T	XM_047450086.1:c.409-2690C>G	XM_047450086.1:c.409-2690C>A
RNF212 transcript variant X9	XM_047450087.1:c.379-2690=	XM_047450087.1:c.379-2690C>T	XM_047450087.1:c.379-2690C>G	XM_047450087.1:c.379-2690C>A
RNF212 transcript variant X11	XM_047450088.1:c.343-2690=	XM_047450088.1:c.343-2690C>T	XM_047450088.1:c.343-2690C>G	XM_047450088.1:c.343-2690C>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#.

83 SubSNP, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BCM_SSAHASNP	ss10145991	Jul 11, 2003 (116)
2	CSHL-HAPMAP	ss17006905	Feb 27, 2004 (120)
3	CSHL-HAPMAP	ss20197059	Feb 27, 2004 (120)
4	SSAHASNP	ss22129778	Apr 05, 2004 (123)
5	PERLEGEN	ss23964221	Sep 20, 2004 (123)
6	ABI	ss42209222	Mar 14, 2006 (126)
7	HGSV	ss77591339	Dec 06, 2007 (129)
8	HGSV	ss85563583	Dec 15, 2007 (130)
9	BCMHGSC_JDW	ss92437791	Mar 24, 2008 (129)
10	HUMANGENOME_JCVI	ss98926032	Feb 06, 2009 (130)
11	BGI	ss105798995	Feb 06, 2009 (130)
12	1000GENOMES	ss111650883	Jan 25, 2009 (130)
13	1000GENOMES	ss112843898	Jan 25, 2009 (130)
14	ILLUMINA-UK	ss116835625	Feb 14, 2009 (130)
15	ENSEMBL	ss135196404	Dec 01, 2009 (131)
16	ENSEMBL	ss139392556	Dec 01, 2009 (131)
17	GMI	ss156739965	Dec 01, 2009 (131)
18	ILLUMINA	ss161080156	Dec 01, 2009 (131)
19	COMPLETE_GENOMICS	ss161887392	Jul 04, 2010 (132)
20	COMPLETE_GENOMICS	ss162990666	Jul 04, 2010 (132)
21	COMPLETE_GENOMICS	ss165991085	Jul 04, 2010 (132)
22	BUSHMAN	ss197889497	Jul 04, 2010 (132)
23	BCM-HGSC-SUB	ss206437648	Jul 04, 2010 (132)
24	1000GENOMES	ss220691006	Jul 14, 2010 (132)
25	1000GENOMES	ss232223466	Jul 14, 2010 (132)
26	1000GENOMES	ss239552777	Jul 15, 2010 (132)
27	BL	ss252870983	May 09, 2011 (134)
28	GMI	ss277537620	May 04, 2012 (137)
29	GMI	ss284828742	Apr 25, 2013 (138)
30	PJP	ss293053024	May 09, 2011 (134)
31	ILLUMINA	ss479425892	Sep 08, 2015 (146)
32	TISHKOFF	ss557250733	Apr 25, 2013 (138)
33	SSMP	ss651003762	Apr 25, 2013 (138)
34	EVA-GONL	ss979668008	Aug 21, 2014 (142)
35	JMKIDD_LAB	ss1071212041	Aug 21, 2014 (142)
36	1000GENOMES	ss1308068589	Aug 21, 2014 (142)
37	DDI	ss1429738095	Apr 01, 2015 (144)
38	EVA_GENOME_DK	ss1580378579	Apr 01, 2015 (144)
39	EVA_DECODE	ss1589164666	Apr 01, 2015 (144)
40	EVA_UK10K_ALSPAC	ss1609226635	Apr 01, 2015 (144)
41	EVA_UK10K_TWINSUK	ss1652220668	Apr 01, 2015 (144)
42	HAMMER_LAB	ss1800784873	Sep 08, 2015 (146)
43	WEILL_CORNELL_DGM	ss1922898263	Feb 12, 2016 (147)
44	GENOMED	ss1969636497	Jul 19, 2016 (147)
45	JJLAB	ss2022023156	Sep 14, 2016 (149)
46	USC_VALOUEV	ss2150128688	Dec 20, 2016 (150)
47	HUMAN_LONGEVITY	ss2259782989	Dec 20, 2016 (150)
48	SYSTEMSBIOZJU	ss2625512516	Nov 08, 2017 (151)
49	GRF	ss2705563140	Nov 08, 2017 (151)
50	GNOMAD	ss2804631453	Nov 08, 2017 (151)
51	SWEGEN	ss2993984416	Nov 08, 2017 (151)
52	BIOINF_KMB_FNS_UNIBA	ss3024781257	Nov 08, 2017 (151)
53	CSHL	ss3345495822	Nov 08, 2017 (151)
54	ILLUMINA	ss3636635538	Oct 12, 2018 (152)
55	URBANLAB	ss3647631485	Oct 12, 2018 (152)
56	EGCUT_WGS	ss3661923166	Jul 13, 2019 (153)
57	EVA_DECODE	ss3711226199	Jul 13, 2019 (153)
58	ACPOP	ss3730773887	Jul 13, 2019 (153)
59	EVA	ss3761278387	Jul 13, 2019 (153)
60	PACBIO	ss3784593315	Jul 13, 2019 (153)
61	PACBIO	ss3790066971	Jul 13, 2019 (153)
62	PACBIO	ss3794942026	Jul 13, 2019 (153)
63	KHV_HUMAN_GENOMES	ss3804418485	Jul 13, 2019 (153)
64	EVA	ss3828323537	Apr 25, 2020 (154)
65	EVA	ss3837593061	Apr 25, 2020 (154)
66	EVA	ss3843026312	Apr 25, 2020 (154)
67	SGDP_PRJ	ss3858011470	Apr 25, 2020 (154)
68	KRGDB	ss3904136414	Apr 25, 2020 (154)
69	TOPMED	ss4600014182	Apr 26, 2021 (155)
70	TOMMO_GENOMICS	ss5163793553	Apr 26, 2021 (155)
71	1000G_HIGH_COVERAGE	ss5257724149	Oct 17, 2022 (156)
72	EVA	ss5346339590	Oct 17, 2022 (156)
73	HUGCELL_USP	ss5456681455	Oct 17, 2022 (156)
74	EVA	ss5507366645	Oct 17, 2022 (156)
75	1000G_HIGH_COVERAGE	ss5538014793	Oct 17, 2022 (156)
76	SANFORD_IMAGENETICS	ss5634163678	Oct 17, 2022 (156)
77	TOMMO_GENOMICS	ss5697319984	Oct 17, 2022 (156)
78	YY_MCH	ss5804673073	Oct 17, 2022 (156)
79	EVA	ss5843421429	Oct 17, 2022 (156)
80	EVA	ss5854044261	Oct 17, 2022 (156)
81	EVA	ss5861796294	Oct 17, 2022 (156)
82	EVA	ss5962539537	Oct 17, 2022 (156)
83	EVA	ss5980199897	Oct 17, 2022 (156)
84	1000Genomes	NC_000004.11 - 1070140	Oct 12, 2018 (152)
85	1000Genomes_30x	NC_000004.12 - 1076352	Oct 17, 2022 (156)
86	The Avon Longitudinal Study of Parents and Children	NC_000004.11 - 1070140	Oct 12, 2018 (152)
87	Genetic variation in the Estonian population	NC_000004.11 - 1070140	Oct 12, 2018 (152)
88	The Danish reference pan genome	NC_000004.11 - 1070140	Apr 25, 2020 (154)
89	gnomAD - Genomes	NC_000004.12 - 1076352	Apr 26, 2021 (155)
90	Genome of the Netherlands Release 5	NC_000004.11 - 1070140	Apr 25, 2020 (154)
91	KOREAN population from KRGDB	NC_000004.11 - 1070140	Apr 25, 2020 (154)
92	Northern Sweden	NC_000004.11 - 1070140	Jul 13, 2019 (153)
93	Qatari	NC_000004.11 - 1070140	Apr 25, 2020 (154)
94	SGDP_PRJ	NC_000004.11 - 1070140	Apr 25, 2020 (154)
95	Siberian	NC_000004.11 - 1070140	Apr 25, 2020 (154)
96	8.3KJPN	NC_000004.11 - 1070140	Apr 26, 2021 (155)
97	14KJPN	NC_000004.12 - 1076352	Oct 17, 2022 (156)
98	TopMed	NC_000004.12 - 1076352	Apr 26, 2021 (155)
99	UK 10K study - Twins	NC_000004.11 - 1070140	Oct 12, 2018 (152)
100	A Vietnamese Genetic Variation Database	NC_000004.11 - 1070140	Jul 13, 2019 (153)
101	ALFA	NC_000004.12 - 1076352	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)
rs13127983	Sep 24, 2004 (123)
rs17164214	Oct 07, 2004 (123)
rs60230241	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
11313808, ss3904136414	NC_000004.11:1070139:G:A	NC_000004.12:1076351:G:A	(self)
11313808, ss3904136414	NC_000004.11:1070139:G:C	NC_000004.12:1076351:G:C	(self)
ss77591339, ss85563583	NC_000004.9:1059969:G:T	NC_000004.12:1076351:G:T	(self)
ss92437791, ss111650883, ss112843898, ss116835625, ss161887392, ss162990666, ss165991085, ss197889497, ss206437648, ss252870983, ss277537620, ss284828742, ss293053024, ss1589164666	NC_000004.10:1060139:G:T	NC_000004.12:1076351:G:T	(self)
19405905, 10817868, 7661414, 6543518, 4754881, 11313808, 4058752, 4940193, 10028450, 2645042, 21762860, 10817868, 2365435, ss220691006, ss232223466, ss239552777, ss479425892, ss557250733, ss651003762, ss979668008, ss1071212041, ss1308068589, ss1429738095, ss1580378579, ss1609226635, ss1652220668, ss1800784873, ss1922898263, ss1969636497, ss2022023156, ss2150128688, ss2625512516, ss2705563140, ss2804631453, ss2993984416, ss3345495822, ss3636635538, ss3661923166, ss3730773887, ss3761278387, ss3784593315, ss3790066971, ss3794942026, ss3828323537, ss3837593061, ss3858011470, ss3904136414, ss5163793553, ss5346339590, ss5507366645, ss5634163678, ss5843421429, ss5962539537, ss5980199897	NC_000004.11:1070139:G:T	NC_000004.12:1076351:G:T	(self)
25540728, 137767546, 31157088, 437391738, 13015935826, ss2259782989, ss3024781257, ss3647631485, ss3711226199, ss3804418485, ss3843026312, ss4600014182, ss5257724149, ss5456681455, ss5538014793, ss5697319984, ss5804673073, ss5854044261, ss5861796294	NC_000004.12:1076351:G:T	NC_000004.12:1076351:G:T	(self)
ss10145991, ss17006905, ss20197059, ss22129778	NT_037622.3:1059969:G:T	NC_000004.12:1076351:G:T	(self)
ss23964221, ss42209222, ss98926032, ss105798995, ss135196404, ss139392556, ss156739965, ss161080156	NT_037622.5:1060139:G:T	NC_000004.12:1076351: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 rs6835141

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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs6835141