Name: rs6010
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.

rs6010

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:169530972 (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>C
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.061661 (16321/264690, TOPMED)
C=0.078934 (19785/250652, GnomAD_exome)
C=0.047678 (7540/158144, ALFA) (+ 21 more)
C=0.049083 (6881/140190, GnomAD)
C=0.074063 (8965/121046, ExAC)
C=0.15423 (4358/28256, 14KJPN)
C=0.15346 (2572/16760, 8.3KJPN)
C=0.03983 (518/13006, GO-ESP)
C=0.0943 (604/6404, 1000G_30x)
C=0.0974 (488/5008, 1000G)
C=0.0283 (127/4480, Estonian)
C=0.0413 (159/3854, ALSPAC)
C=0.0429 (159/3708, TWINSUK)
C=0.1676 (491/2930, KOREAN)
C=0.033 (33/998, GoNL)
C=0.166 (101/609, Vietnamese)
C=0.043 (26/600, NorthernSweden)
C=0.067 (36/534, MGP)
C=0.030 (9/304, FINRISK)
C=0.111 (24/216, Qatari)
T=0.412 (47/114, SGDP_PRJ)
C=0.05 (2/40, GENOME_DK)
T=0.50 (8/16, Siberian)
C=0.50 (8/16, Siberian)

Clinical Significance: Reported in ClinVar
Gene : Consequence: F5 : Synonymous 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	174402	T=0.953475	C=0.046525
European	Sub	137498	T=0.960669	C=0.039331
African	Sub	14698	T=0.96129	C=0.03871
African Others	Sub	512	T=0.957	C=0.043
African American	Sub	14186	T=0.96144	C=0.03856
Asian	Sub	676	T=0.862	C=0.138
East Asian	Sub	514	T=0.840	C=0.160
Other Asian	Sub	162	T=0.932	C=0.068
Latin American 1	Sub	1088	T=0.9265	C=0.0735
Latin American 2	Sub	6276	T=0.8121	C=0.1879
South Asian	Sub	184	T=0.880	C=0.120
Other	Sub	13982	T=0.94543	C=0.05457

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=0.938339	C=0.061661
gnomAD - Exomes	Global	Study-wide	250652	T=0.921066	C=0.078934
gnomAD - Exomes	European	Sub	134724	T=0.962085	C=0.037915
gnomAD - Exomes	Asian	Sub	48990	T=0.88175	C=0.11825
gnomAD - Exomes	American	Sub	34536	T=0.79314	C=0.20686
gnomAD - Exomes	African	Sub	16248	T=0.96104	C=0.03896
gnomAD - Exomes	Ashkenazi Jewish	Sub	10052	T=0.93156	C=0.06844
gnomAD - Exomes	Other	Sub	6102	T=0.9313	C=0.0687
Allele Frequency Aggregator	Total	Global	158144	T=0.952322	C=0.047678
Allele Frequency Aggregator	European	Sub	127488	T=0.960184	C=0.039816
Allele Frequency Aggregator	Other	Sub	12558	T=0.94362	C=0.05638
Allele Frequency Aggregator	African	Sub	9874	T=0.9613	C=0.0387
Allele Frequency Aggregator	Latin American 2	Sub	6276	T=0.8121	C=0.1879
Allele Frequency Aggregator	Latin American 1	Sub	1088	T=0.9265	C=0.0735
Allele Frequency Aggregator	Asian	Sub	676	T=0.862	C=0.138
Allele Frequency Aggregator	South Asian	Sub	184	T=0.880	C=0.120
gnomAD - Genomes	Global	Study-wide	140190	T=0.950917	C=0.049083
gnomAD - Genomes	European	Sub	75916	T=0.96248	C=0.03752
gnomAD - Genomes	African	Sub	42030	T=0.96053	C=0.03947
gnomAD - Genomes	American	Sub	13644	T=0.88515	C=0.11485
gnomAD - Genomes	Ashkenazi Jewish	Sub	3320	T=0.9343	C=0.0657
gnomAD - Genomes	East Asian	Sub	3132	T=0.8544	C=0.1456
gnomAD - Genomes	Other	Sub	2148	T=0.9381	C=0.0619
ExAC	Global	Study-wide	121046	T=0.925937	C=0.074063
ExAC	Europe	Sub	73170	T=0.96048	C=0.03952
ExAC	Asian	Sub	25126	T=0.88152	C=0.11848
ExAC	American	Sub	11502	T=0.77013	C=0.22987
ExAC	African	Sub	10340	T=0.96209	C=0.03791
ExAC	Other	Sub	908	T=0.934	C=0.066
14KJPN	JAPANESE	Study-wide	28256	T=0.84577	C=0.15423
8.3KJPN	JAPANESE	Study-wide	16760	T=0.84654	C=0.15346
GO Exome Sequencing Project	Global	Study-wide	13006	T=0.96017	C=0.03983
GO Exome Sequencing Project	European American	Sub	8600	T=0.9597	C=0.0403
GO Exome Sequencing Project	African American	Sub	4406	T=0.9612	C=0.0388
1000Genomes_30x	Global	Study-wide	6404	T=0.9057	C=0.0943
1000Genomes_30x	African	Sub	1786	T=0.9636	C=0.0364
1000Genomes_30x	Europe	Sub	1266	T=0.9629	C=0.0371
1000Genomes_30x	South Asian	Sub	1202	T=0.8877	C=0.1123
1000Genomes_30x	East Asian	Sub	1170	T=0.8256	C=0.1744
1000Genomes_30x	American	Sub	980	T=0.844	C=0.156
1000Genomes	Global	Study-wide	5008	T=0.9026	C=0.0974
1000Genomes	African	Sub	1322	T=0.9622	C=0.0378
1000Genomes	East Asian	Sub	1008	T=0.8294	C=0.1706
1000Genomes	Europe	Sub	1006	T=0.9602	C=0.0398
1000Genomes	South Asian	Sub	978	T=0.883	C=0.117
1000Genomes	American	Sub	694	T=0.839	C=0.161
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.9717	C=0.0283
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.9587	C=0.0413
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.9571	C=0.0429
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.8324	C=0.1676
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.967	C=0.033
A Vietnamese Genetic Variation Database	Global	Study-wide	609	T=0.834	C=0.166
Northern Sweden	ACPOP	Study-wide	600	T=0.957	C=0.043
Medical Genome Project healthy controls from Spanish population	Spanish controls	Study-wide	534	T=0.933	C=0.067
FINRISK	Finnish from FINRISK project	Study-wide	304	T=0.970	C=0.030
Qatari	Global	Study-wide	216	T=0.889	C=0.111
SGDP_PRJ	Global	Study-wide	114	T=0.412	C=0.588
The Danish reference pan genome	Danish	Study-wide	40	T=0.95	C=0.05
Siberian	Global	Study-wide	16	T=0.50	C=0.50

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.169530972T>C
GRCh37.p13 chr 1	NC_000001.10:g.169500210T>C
F5 RefSeqGene (LRG_553)	NG_011806.1:g.60560A>G

Gene: F5, coagulation factor V (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
F5 transcript	NM_000130.5:c.5022A>G	G [GGA] > G [GGG]	Coding Sequence Variant
coagulation factor V preproprotein	NP_000121.2:p.Gly1674=	G (Gly) > G (Gly)	Synonymous 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.

Allele: C (allele ID: 278298 )

ClinVar Accession	Disease Names	Clinical Significance
RCV000281808.3	Budd-Chiari syndrome	Benign
RCV000331051.3	Thrombophilia due to activated protein C resistance	Likely-Benign
RCV000385446.3	Factor V deficiency	Benign
RCV000400931.3	Thrombophilia due to thrombin defect	Benign
RCV001668641.2	not provided	Benign

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=	C
GRCh38.p14 chr 1	NC_000001.11:g.169530972=	NC_000001.11:g.169530972T>C
GRCh37.p13 chr 1	NC_000001.10:g.169500210=	NC_000001.10:g.169500210T>C
F5 RefSeqGene (LRG_553)	NG_011806.1:g.60560=	NG_011806.1:g.60560A>G
F5 transcript	NM_000130.5:c.5022=	NM_000130.5:c.5022A>G
F5 transcript	NM_000130.4:c.5022=	NM_000130.4:c.5022A>G
coagulation factor V preproprotein	NP_000121.2:p.Gly1674=	NP_000121.2:p.Gly1674=

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#.

105 SubSNP, 23 Frequency, 5 ClinVar submissions

No	Submitter	Submission ID	Date (Build)
1	WIAF-CSNP	ss7620	Sep 19, 2000 (52)
2	PGA-UW-FHCRC	ss12674319	Dec 05, 2003 (119)
3	SC_SNP	ss15384059	Feb 27, 2004 (120)
4	IMCJ-GDT	ss22887070	Apr 05, 2004 (121)
5	SI_EXO	ss52080113	Oct 14, 2006 (127)
6	PGA-UW-FHCRC	ss52086748	Oct 14, 2006 (127)
7	SEATTLESEQ	ss159699588	Dec 01, 2009 (131)
8	ILLUMINA	ss160756996	Dec 01, 2009 (131)
9	COMPLETE_GENOMICS	ss165406256	Jul 04, 2010 (132)
10	ILLUMINA	ss173961653	Jul 04, 2010 (132)
11	1000GENOMES	ss218708042	Jul 14, 2010 (132)
12	1000GENOMES	ss238413555	Jul 15, 2010 (132)
13	ILLUMINA	ss244304091	Jul 04, 2010 (132)
14	GMI	ss276094657	May 04, 2012 (137)
15	NHLBI-ESP	ss342009881	May 09, 2011 (134)
16	ILLUMINA	ss481190314	May 04, 2012 (137)
17	ILLUMINA	ss481213293	May 04, 2012 (137)
18	ILLUMINA	ss482200686	Sep 08, 2015 (146)
19	ILLUMINA	ss485390342	May 04, 2012 (137)
20	1000GENOMES	ss489776479	May 04, 2012 (137)
21	CLINSEQ_SNP	ss491609135	May 04, 2012 (137)
22	ILLUMINA	ss537329780	Sep 08, 2015 (146)
23	SSMP	ss648486948	Apr 25, 2013 (138)
24	ILLUMINA	ss780676367	Aug 21, 2014 (142)
25	ILLUMINA	ss783140712	Sep 08, 2015 (146)
26	ILLUMINA	ss784096951	Aug 21, 2014 (142)
27	ILLUMINA	ss832399790	Sep 08, 2015 (146)
28	ILLUMINA	ss836172769	Aug 21, 2014 (142)
29	EVA-GONL	ss975794245	Aug 21, 2014 (142)
30	JMKIDD_LAB	ss1067428614	Aug 21, 2014 (142)
31	JMKIDD_LAB	ss1068350521	Aug 21, 2014 (142)
32	1000GENOMES	ss1293348069	Aug 21, 2014 (142)
33	EVA_GENOME_DK	ss1574463691	Apr 01, 2015 (144)
34	EVA_FINRISK	ss1584012764	Apr 01, 2015 (144)
35	EVA_DECODE	ss1585179750	Apr 01, 2015 (144)
36	EVA_UK10K_ALSPAC	ss1601439193	Apr 01, 2015 (144)
37	EVA_UK10K_TWINSUK	ss1644433226	Apr 01, 2015 (144)
38	EVA_EXAC	ss1685903024	Apr 01, 2015 (144)
39	EVA_MGP	ss1710931926	Apr 01, 2015 (144)
40	ILLUMINA	ss1751880328	Sep 08, 2015 (146)
41	WEILL_CORNELL_DGM	ss1919030886	Feb 12, 2016 (147)
42	GENOMED	ss1966894202	Jul 19, 2016 (147)
43	JJLAB	ss2020031223	Sep 14, 2016 (149)
44	ILLUMINA	ss2094784998	Dec 20, 2016 (150)
45	USC_VALOUEV	ss2148058608	Dec 20, 2016 (150)
46	HUMAN_LONGEVITY	ss2167387139	Dec 20, 2016 (150)
47	SYSTEMSBIOZJU	ss2624524856	Nov 08, 2017 (151)
48	ILLUMINA	ss2632590727	Nov 08, 2017 (151)
49	GRF	ss2698036764	Nov 08, 2017 (151)
50	GNOMAD	ss2746493663	Nov 08, 2017 (151)
51	GNOMAD	ss2762502842	Nov 08, 2017 (151)
52	SWEGEN	ss2987923821	Nov 08, 2017 (151)
53	BIOINF_KMB_FNS_UNIBA	ss3023773621	Nov 08, 2017 (151)
54	CSHL	ss3343761043	Nov 08, 2017 (151)
55	ILLUMINA	ss3626236137	Oct 11, 2018 (152)
56	ILLUMINA	ss3630622636	Oct 11, 2018 (152)
57	ILLUMINA	ss3632914430	Oct 11, 2018 (152)
58	ILLUMINA	ss3633609974	Oct 11, 2018 (152)
59	ILLUMINA	ss3634357256	Oct 11, 2018 (152)
60	ILLUMINA	ss3635303332	Oct 11, 2018 (152)
61	ILLUMINA	ss3636036279	Oct 11, 2018 (152)
62	ILLUMINA	ss3637053831	Oct 11, 2018 (152)
63	ILLUMINA	ss3637794595	Oct 11, 2018 (152)
64	ILLUMINA	ss3640064610	Oct 11, 2018 (152)
65	OMUKHERJEE_ADBS	ss3646248613	Oct 11, 2018 (152)
66	EGCUT_WGS	ss3655866984	Jul 12, 2019 (153)
67	EVA_DECODE	ss3687989518	Jul 12, 2019 (153)
68	ACPOP	ss3727579154	Jul 12, 2019 (153)
69	ILLUMINA	ss3744658134	Jul 12, 2019 (153)
70	EVA	ss3746937824	Jul 12, 2019 (153)
71	ILLUMINA	ss3772159188	Jul 12, 2019 (153)
72	PACBIO	ss3783597364	Jul 12, 2019 (153)
73	PACBIO	ss3789223967	Jul 12, 2019 (153)
74	PACBIO	ss3794096029	Jul 12, 2019 (153)
75	KHV_HUMAN_GENOMES	ss3799939254	Jul 12, 2019 (153)
76	EVA	ss3823683512	Apr 25, 2020 (154)
77	EVA	ss3825580168	Apr 25, 2020 (154)
78	EVA	ss3826480522	Apr 25, 2020 (154)
79	EVA	ss3836636378	Apr 25, 2020 (154)
80	EVA	ss3842046258	Apr 25, 2020 (154)
81	SGDP_PRJ	ss3850224652	Apr 25, 2020 (154)
82	KRGDB	ss3895460454	Apr 25, 2020 (154)
83	FSA-LAB	ss3983953141	Apr 25, 2021 (155)
84	FSA-LAB	ss3983953142	Apr 25, 2021 (155)
85	EVA	ss3986146480	Apr 25, 2021 (155)
86	EVA	ss4016944540	Apr 25, 2021 (155)
87	TOPMED	ss4471976251	Apr 25, 2021 (155)
88	TOMMO_GENOMICS	ss5146958960	Apr 25, 2021 (155)
89	EVA	ss5236875515	Apr 25, 2021 (155)
90	EVA	ss5237633383	Oct 12, 2022 (156)
91	1000G_HIGH_COVERAGE	ss5244658237	Oct 12, 2022 (156)
92	TRAN_CS_UWATERLOO	ss5314397963	Oct 12, 2022 (156)
93	EVA	ss5322717805	Oct 12, 2022 (156)
94	HUGCELL_USP	ss5445207324	Oct 12, 2022 (156)
95	1000G_HIGH_COVERAGE	ss5518169660	Oct 12, 2022 (156)
96	SANFORD_IMAGENETICS	ss5626801836	Oct 12, 2022 (156)
97	TOMMO_GENOMICS	ss5674294780	Oct 12, 2022 (156)
98	EVA	ss5799502504	Oct 12, 2022 (156)
99	YY_MCH	ss5801353204	Oct 12, 2022 (156)
100	EVA	ss5832811613	Oct 12, 2022 (156)
101	EVA	ss5848277506	Oct 12, 2022 (156)
102	EVA	ss5849152989	Oct 12, 2022 (156)
103	EVA	ss5910664616	Oct 12, 2022 (156)
104	EVA	ss5938603551	Oct 12, 2022 (156)
105	EVA	ss5981198622	Oct 12, 2022 (156)
106	1000Genomes	NC_000001.10 - 169500210	Oct 11, 2018 (152)
107	1000Genomes_30x	NC_000001.11 - 169530972	Oct 12, 2022 (156)
108	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 169500210	Oct 11, 2018 (152)
109	Genetic variation in the Estonian population	NC_000001.10 - 169500210	Oct 11, 2018 (152)
110	ExAC	NC_000001.10 - 169500210	Oct 11, 2018 (152)
111	FINRISK	NC_000001.10 - 169500210	Apr 25, 2020 (154)
112	The Danish reference pan genome	NC_000001.10 - 169500210	Apr 25, 2020 (154)
113	gnomAD - Genomes	NC_000001.11 - 169530972	Apr 25, 2021 (155)
114	gnomAD - Exomes	NC_000001.10 - 169500210	Jul 12, 2019 (153)
115	GO Exome Sequencing Project	NC_000001.10 - 169500210	Oct 11, 2018 (152)
116	Genome of the Netherlands Release 5	NC_000001.10 - 169500210	Apr 25, 2020 (154)
117	KOREAN population from KRGDB	NC_000001.10 - 169500210	Apr 25, 2020 (154)
118	Medical Genome Project healthy controls from Spanish population	NC_000001.10 - 169500210	Apr 25, 2020 (154)
119	Northern Sweden	NC_000001.10 - 169500210	Jul 12, 2019 (153)
120	Qatari	NC_000001.10 - 169500210	Apr 25, 2020 (154)
121	SGDP_PRJ	NC_000001.10 - 169500210	Apr 25, 2020 (154)
122	Siberian	NC_000001.10 - 169500210	Apr 25, 2020 (154)
123	8.3KJPN	NC_000001.10 - 169500210	Apr 25, 2021 (155)
124	14KJPN	NC_000001.11 - 169530972	Oct 12, 2022 (156)
125	TopMed	NC_000001.11 - 169530972	Apr 25, 2021 (155)
126	UK 10K study - Twins	NC_000001.10 - 169500210	Oct 11, 2018 (152)
127	A Vietnamese Genetic Variation Database	NC_000001.10 - 169500210	Jul 12, 2019 (153)
128	ALFA	NC_000001.11 - 169530972	Apr 25, 2021 (155)
129	ClinVar	RCV000281808.3	Oct 12, 2022 (156)
130	ClinVar	RCV000331051.3	Oct 12, 2022 (156)
131	ClinVar	RCV000385446.3	Oct 12, 2022 (156)
132	ClinVar	RCV000400931.3	Oct 12, 2022 (156)
133	ClinVar	RCV001668641.2	Oct 12, 2022 (156)

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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss165406256, ss276094657, ss481190314, ss491609135, ss1585179750	NC_000001.9:167766833:T:C	NC_000001.11:169530971:T:C	(self)
4154491, 2268120, 1605232, 5128287, 9225, 1752377, 1069865, 142077, 986544, 2637848, 48678, 864019, 1072816, 2241632, 574962, 4928267, 2268120, 487831, ss218708042, ss238413555, ss342009881, ss481213293, ss482200686, ss485390342, ss489776479, ss537329780, ss648486948, ss780676367, ss783140712, ss784096951, ss832399790, ss836172769, ss975794245, ss1067428614, ss1068350521, ss1293348069, ss1574463691, ss1584012764, ss1601439193, ss1644433226, ss1685903024, ss1710931926, ss1751880328, ss1919030886, ss1966894202, ss2020031223, ss2094784998, ss2148058608, ss2624524856, ss2632590727, ss2698036764, ss2746493663, ss2762502842, ss2987923821, ss3343761043, ss3626236137, ss3630622636, ss3632914430, ss3633609974, ss3634357256, ss3635303332, ss3636036279, ss3637053831, ss3637794595, ss3640064610, ss3646248613, ss3655866984, ss3727579154, ss3744658134, ss3746937824, ss3772159188, ss3783597364, ss3789223967, ss3794096029, ss3823683512, ss3825580168, ss3826480522, ss3836636378, ss3850224652, ss3895460454, ss3983953141, ss3983953142, ss3986146480, ss4016944540, ss5146958960, ss5322717805, ss5626801836, ss5799502504, ss5832811613, ss5848277506, ss5938603551, ss5981198622	NC_000001.10:169500209:T:C	NC_000001.11:169530971:T:C	(self)
RCV000281808.3, RCV000331051.3, RCV000385446.3, RCV000400931.3, RCV001668641.2, 5695595, 30068249, 8131884, 35582586, 11260415129, ss2167387139, ss3023773621, ss3687989518, ss3799939254, ss3842046258, ss4471976251, ss5236875515, ss5237633383, ss5244658237, ss5314397963, ss5445207324, ss5518169660, ss5674294780, ss5801353204, ss5849152989, ss5910664616	NC_000001.11:169530971:T:C	NC_000001.11:169530971:T:C	(self)
ss52080113	NT_004487.17:19909149:T:C	NC_000001.11:169530971:T:C	(self)
ss7620, ss12674319, ss22887070, ss52086748, ss159699588, ss160756996, ss173961653, ss244304091	NT_004487.19:20988851:T:C	NC_000001.11:169530971:T:C	(self)
ss15384059	NT_004668.16:8005681:T:C	NC_000001.11:169530971: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 rs6010

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

rs6010