Name: rs10006043
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.

rs10006043

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:76436594 (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=0.480728 (127244/264690, TOPMED)
C=0.457409 (71976/157356, ALFA)
T=0.496807 (69541/139976, GnomAD) (+ 18 more)
T=0.27196 (7685/28258, 14KJPN)
T=0.27076 (4538/16760, 8.3KJPN)
T=0.4168 (2669/6404, 1000G_30x)
T=0.4153 (2080/5008, 1000G)
C=0.3842 (1721/4480, Estonian)
C=0.4403 (1697/3854, ALSPAC)
C=0.4393 (1629/3708, TWINSUK)
T=0.2652 (777/2930, KOREAN)
T=0.4203 (876/2084, HGDP_Stanford)
T=0.4063 (768/1890, HapMap)
C=0.434 (433/998, GoNL)
C=0.390 (234/600, NorthernSweden)
C=0.361 (119/330, SGDP_PRJ)
T=0.440 (95/216, Qatari)
T=0.330 (70/212, Vietnamese)
C=0.36 (15/42, Siberian)
C=0.47 (19/40, GENOME_DK)
T=0.2 (2/8, Ancient Sardinia)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SHROOM3 : 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	157356	C=0.457409	T=0.542591
European	Sub	136522	C=0.443218	T=0.556782
African	Sub	6682	C=0.5910	T=0.4090
African Others	Sub	242	C=0.632	T=0.368
African American	Sub	6440	C=0.5894	T=0.4106
Asian	Sub	636	C=0.671	T=0.329
East Asian	Sub	504	C=0.659	T=0.341
Other Asian	Sub	132	C=0.720	T=0.280
Latin American 1	Sub	758	C=0.497	T=0.503
Latin American 2	Sub	6330	C=0.5586	T=0.4414
South Asian	Sub	184	C=0.576	T=0.424
Other	Sub	6244	C=0.4920	T=0.5080

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	C=0.519272	T=0.480728
Allele Frequency Aggregator	Total	Global	157356	C=0.457409	T=0.542591
Allele Frequency Aggregator	European	Sub	136522	C=0.443218	T=0.556782
Allele Frequency Aggregator	African	Sub	6682	C=0.5910	T=0.4090
Allele Frequency Aggregator	Latin American 2	Sub	6330	C=0.5586	T=0.4414
Allele Frequency Aggregator	Other	Sub	6244	C=0.4920	T=0.5080
Allele Frequency Aggregator	Latin American 1	Sub	758	C=0.497	T=0.503
Allele Frequency Aggregator	Asian	Sub	636	C=0.671	T=0.329
Allele Frequency Aggregator	South Asian	Sub	184	C=0.576	T=0.424
gnomAD - Genomes	Global	Study-wide	139976	C=0.503193	T=0.496807
gnomAD - Genomes	European	Sub	75826	C=0.43972	T=0.56028
gnomAD - Genomes	African	Sub	41918	C=0.59562	T=0.40438
gnomAD - Genomes	American	Sub	13632	C=0.55421	T=0.44579
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	C=0.4398	T=0.5602
gnomAD - Genomes	East Asian	Sub	3128	C=0.6439	T=0.3561
gnomAD - Genomes	Other	Sub	2148	C=0.5098	T=0.4902
14KJPN	JAPANESE	Study-wide	28258	C=0.72804	T=0.27196
8.3KJPN	JAPANESE	Study-wide	16760	C=0.72924	T=0.27076
1000Genomes_30x	Global	Study-wide	6404	C=0.5832	T=0.4168
1000Genomes_30x	African	Sub	1786	C=0.6153	T=0.3847
1000Genomes_30x	Europe	Sub	1266	C=0.4629	T=0.5371
1000Genomes_30x	South Asian	Sub	1202	C=0.6206	T=0.3794
1000Genomes_30x	East Asian	Sub	1170	C=0.6333	T=0.3667
1000Genomes_30x	American	Sub	980	C=0.574	T=0.426
1000Genomes	Global	Study-wide	5008	C=0.5847	T=0.4153
1000Genomes	African	Sub	1322	C=0.6120	T=0.3880
1000Genomes	East Asian	Sub	1008	C=0.6349	T=0.3651
1000Genomes	Europe	Sub	1006	C=0.4662	T=0.5338
1000Genomes	South Asian	Sub	978	C=0.623	T=0.377
1000Genomes	American	Sub	694	C=0.578	T=0.422
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.3842	T=0.6158
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.4403	T=0.5597
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.4393	T=0.5607
KOREAN population from KRGDB	KOREAN	Study-wide	2930	C=0.7348	T=0.2652
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	C=0.5797	T=0.4203
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	C=0.687	T=0.313
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	C=0.618	T=0.382
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	C=0.571	T=0.429
HGDP-CEPH-db Supplement 1	Europe	Sub	320	C=0.412	T=0.588
HGDP-CEPH-db Supplement 1	Africa	Sub	242	C=0.442	T=0.558
HGDP-CEPH-db Supplement 1	America	Sub	216	C=0.620	T=0.380
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	C=0.78	T=0.22
HapMap	Global	Study-wide	1890	C=0.5937	T=0.4063
HapMap	American	Sub	770	C=0.566	T=0.434
HapMap	African	Sub	692	C=0.614	T=0.386
HapMap	Asian	Sub	252	C=0.679	T=0.321
HapMap	Europe	Sub	176	C=0.511	T=0.489
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.434	T=0.566
Northern Sweden	ACPOP	Study-wide	600	C=0.390	T=0.610
SGDP_PRJ	Global	Study-wide	330	C=0.361	T=0.639
Qatari	Global	Study-wide	216	C=0.560	T=0.440
A Vietnamese Genetic Variation Database	Global	Study-wide	212	C=0.670	T=0.330
Siberian	Global	Study-wide	42	C=0.36	T=0.64
The Danish reference pan genome	Danish	Study-wide	40	C=0.47	T=0.53
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	8	C=0.8	T=0.2

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.76436594C>T
GRCh37.p13 chr 4	NC_000004.11:g.77357747C>T
SHROOM3 RefSeqGene	NG_028077.1:g.6495C>T

Gene: SHROOM3, shroom family member 3 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SHROOM3 transcript	NM_020859.4:c.168+374C>T	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	C=	T
GRCh38.p14 chr 4	NC_000004.12:g.76436594=	NC_000004.12:g.76436594C>T
GRCh37.p13 chr 4	NC_000004.11:g.77357747=	NC_000004.11:g.77357747C>T
SHROOM3 RefSeqGene	NG_028077.1:g.6495=	NG_028077.1:g.6495C>T
SHROOM3 transcript	NM_020859.3:c.168+374=	NM_020859.3:c.168+374C>T
SHROOM3 transcript	NM_020859.4:c.168+374=	NM_020859.4:c.168+374C>T
SHROOM3 transcript variant X1	XM_005263162.1:c.168+374=	XM_005263162.1:c.168+374C>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#.

119 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	WI_SSAHASNP	ss13851964	Dec 05, 2003 (119)
2	CSHL-HAPMAP	ss17791363	Feb 27, 2004 (120)
3	ABI	ss44544756	Mar 15, 2006 (126)
4	ILLUMINA	ss65804219	Oct 16, 2006 (127)
5	ILLUMINA	ss66863983	Dec 01, 2006 (127)
6	ILLUMINA	ss66933098	Dec 01, 2006 (127)
7	ILLUMINA	ss68075087	Dec 12, 2006 (127)
8	PERLEGEN	ss68902453	May 17, 2007 (127)
9	ILLUMINA	ss70459336	May 25, 2008 (130)
10	ILLUMINA	ss70979897	May 17, 2007 (127)
11	ILLUMINA	ss75674288	Dec 06, 2007 (129)
12	KRIBB_YJKIM	ss84888515	Dec 15, 2007 (130)
13	HGSV	ss85660512	Dec 15, 2007 (130)
14	BCMHGSC_JDW	ss92650710	Mar 24, 2008 (129)
15	BGI	ss104084588	Dec 01, 2009 (131)
16	1000GENOMES	ss108061306	Jan 22, 2009 (130)
17	ILLUMINA-UK	ss117054561	Feb 14, 2009 (130)
18	ILLUMINA	ss152539387	Dec 01, 2009 (131)
19	GMI	ss157477070	Dec 01, 2009 (131)
20	ILLUMINA	ss159850702	Dec 01, 2009 (131)
21	ENSEMBL	ss161572805	Dec 01, 2009 (131)
22	COMPLETE_GENOMICS	ss163627446	Jul 04, 2010 (132)
23	COMPLETE_GENOMICS	ss166773548	Jul 04, 2010 (132)
24	ILLUMINA	ss169494940	Jul 04, 2010 (132)
25	BUSHMAN	ss198722397	Jul 04, 2010 (132)
26	BCM-HGSC-SUB	ss206564608	Jul 04, 2010 (132)
27	1000GENOMES	ss221010890	Jul 14, 2010 (132)
28	1000GENOMES	ss232453481	Jul 14, 2010 (132)
29	1000GENOMES	ss239733968	Jul 15, 2010 (132)
30	GMI	ss277785061	May 04, 2012 (137)
31	GMI	ss284939147	Apr 25, 2013 (138)
32	PJP	ss293105792	May 09, 2011 (134)
33	ILLUMINA	ss479153993	May 04, 2012 (137)
34	ILLUMINA	ss479155586	May 04, 2012 (137)
35	ILLUMINA	ss479469436	Sep 08, 2015 (146)
36	ILLUMINA	ss484378168	May 04, 2012 (137)
37	ILLUMINA	ss536564505	Sep 08, 2015 (146)
38	TISHKOFF	ss557615357	Apr 25, 2013 (138)
39	SSMP	ss651424008	Apr 25, 2013 (138)
40	ILLUMINA	ss778719356	Sep 08, 2015 (146)
41	ILLUMINA	ss782635371	Sep 08, 2015 (146)
42	ILLUMINA	ss783604918	Sep 08, 2015 (146)
43	ILLUMINA	ss831885446	Sep 08, 2015 (146)
44	ILLUMINA	ss834178736	Sep 08, 2015 (146)
45	EVA-GONL	ss980277329	Aug 21, 2014 (142)
46	JMKIDD_LAB	ss1071661332	Aug 21, 2014 (142)
47	1000GENOMES	ss1310350219	Aug 21, 2014 (142)
48	DDI	ss1429933222	Apr 01, 2015 (144)
49	EVA_GENOME_DK	ss1580622346	Apr 01, 2015 (144)
50	EVA_DECODE	ss1589776647	Apr 01, 2015 (144)
51	EVA_UK10K_ALSPAC	ss1610397689	Apr 01, 2015 (144)
52	EVA_UK10K_TWINSUK	ss1653391722	Apr 01, 2015 (144)
53	EVA_SVP	ss1712682359	Apr 01, 2015 (144)
54	ILLUMINA	ss1752532306	Sep 08, 2015 (146)
55	HAMMER_LAB	ss1801686389	Sep 08, 2015 (146)
56	WEILL_CORNELL_DGM	ss1923520445	Feb 12, 2016 (147)
57	GENOMED	ss1969780408	Jul 19, 2016 (147)
58	JJLAB	ss2022345926	Sep 14, 2016 (149)
59	ILLUMINA	ss2095145053	Dec 20, 2016 (150)
60	USC_VALOUEV	ss2150474472	Dec 20, 2016 (150)
61	HUMAN_LONGEVITY	ss2264098166	Dec 20, 2016 (150)
62	SYSTEMSBIOZJU	ss2625673664	Nov 08, 2017 (151)
63	ILLUMINA	ss2634136450	Nov 08, 2017 (151)
64	GRF	ss2705948482	Nov 08, 2017 (151)
65	GNOMAD	ss2811041841	Nov 08, 2017 (151)
66	SWEGEN	ss2994950792	Nov 08, 2017 (151)
67	BIOINF_KMB_FNS_UNIBA	ss3024947653	Nov 08, 2017 (151)
68	CSHL	ss3345790088	Nov 08, 2017 (151)
69	ILLUMINA	ss3628994227	Oct 12, 2018 (152)
70	ILLUMINA	ss3632071864	Oct 12, 2018 (152)
71	ILLUMINA	ss3633338785	Oct 12, 2018 (152)
72	ILLUMINA	ss3634057922	Oct 12, 2018 (152)
73	ILLUMINA	ss3634957427	Oct 12, 2018 (152)
74	ILLUMINA	ss3635740754	Oct 12, 2018 (152)
75	ILLUMINA	ss3636661113	Oct 12, 2018 (152)
76	ILLUMINA	ss3637493275	Oct 12, 2018 (152)
77	ILLUMINA	ss3638493603	Oct 12, 2018 (152)
78	ILLUMINA	ss3639249412	Oct 12, 2018 (152)
79	ILLUMINA	ss3639923505	Oct 12, 2018 (152)
80	ILLUMINA	ss3640664721	Oct 12, 2018 (152)
81	ILLUMINA	ss3643444363	Oct 12, 2018 (152)
82	ILLUMINA	ss3643969678	Oct 12, 2018 (152)
83	ILLUMINA	ss3652871023	Oct 12, 2018 (152)
84	EGCUT_WGS	ss3662834051	Jul 13, 2019 (153)
85	EVA_DECODE	ss3712346980	Jul 13, 2019 (153)
86	ACPOP	ss3731284800	Jul 13, 2019 (153)
87	ILLUMINA	ss3745257691	Jul 13, 2019 (153)
88	EVA	ss3761981839	Jul 13, 2019 (153)
89	ILLUMINA	ss3772752289	Jul 13, 2019 (153)
90	PACBIO	ss3784760413	Jul 13, 2019 (153)
91	PACBIO	ss3790212032	Jul 13, 2019 (153)
92	PACBIO	ss3795087382	Jul 13, 2019 (153)
93	KHV_HUMAN_GENOMES	ss3805124113	Jul 13, 2019 (153)
94	EVA	ss3828621812	Apr 26, 2020 (154)
95	EVA	ss3837752625	Apr 26, 2020 (154)
96	EVA	ss3843190105	Apr 26, 2020 (154)
97	HGDP	ss3847754288	Apr 26, 2020 (154)
98	SGDP_PRJ	ss3859278103	Apr 26, 2020 (154)
99	KRGDB	ss3905536291	Apr 26, 2020 (154)
100	EVA	ss3985076795	Apr 26, 2021 (155)
101	EVA	ss4017152167	Apr 26, 2021 (155)
102	TOPMED	ss4619083575	Apr 26, 2021 (155)
103	TOMMO_GENOMICS	ss5166386647	Apr 26, 2021 (155)
104	EVA	ss5237351412	Apr 26, 2021 (155)
105	1000G_HIGH_COVERAGE	ss5259736130	Oct 13, 2022 (156)
106	EVA	ss5314967663	Oct 13, 2022 (156)
107	HUGCELL_USP	ss5458436527	Oct 13, 2022 (156)
108	EVA	ss5507578082	Oct 13, 2022 (156)
109	1000G_HIGH_COVERAGE	ss5541107140	Oct 13, 2022 (156)
110	SANFORD_IMAGENETICS	ss5635345961	Oct 13, 2022 (156)
111	TOMMO_GENOMICS	ss5700919738	Oct 13, 2022 (156)
112	EVA	ss5799618378	Oct 13, 2022 (156)
113	YY_MCH	ss5805220082	Oct 13, 2022 (156)
114	EVA	ss5844204297	Oct 13, 2022 (156)
115	EVA	ss5854291219	Oct 13, 2022 (156)
116	EVA	ss5864047675	Oct 13, 2022 (156)
117	EVA	ss5963723908	Oct 13, 2022 (156)
118	EVA	ss5979704215	Oct 13, 2022 (156)
119	EVA	ss5980232670	Oct 13, 2022 (156)
120	1000Genomes	NC_000004.11 - 77357747	Oct 12, 2018 (152)
121	1000Genomes_30x	NC_000004.12 - 76436594	Oct 13, 2022 (156)
122	The Avon Longitudinal Study of Parents and Children	NC_000004.11 - 77357747	Oct 12, 2018 (152)
123	Genetic variation in the Estonian population	NC_000004.11 - 77357747	Oct 12, 2018 (152)
124	The Danish reference pan genome	NC_000004.11 - 77357747	Apr 26, 2020 (154)
125	gnomAD - Genomes	NC_000004.12 - 76436594	Apr 26, 2021 (155)
126	Genome of the Netherlands Release 5	NC_000004.11 - 77357747	Apr 26, 2020 (154)
127	HGDP-CEPH-db Supplement 1	NC_000004.10 - 77576771	Apr 26, 2020 (154)
128	HapMap	NC_000004.12 - 76436594	Apr 26, 2020 (154)
129	KOREAN population from KRGDB	NC_000004.11 - 77357747	Apr 26, 2020 (154)
130	Northern Sweden	NC_000004.11 - 77357747	Jul 13, 2019 (153)
131	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000004.11 - 77357747	Apr 26, 2021 (155)
132	Qatari	NC_000004.11 - 77357747	Apr 26, 2020 (154)
133	SGDP_PRJ	NC_000004.11 - 77357747	Apr 26, 2020 (154)
134	Siberian	NC_000004.11 - 77357747	Apr 26, 2020 (154)
135	8.3KJPN	NC_000004.11 - 77357747	Apr 26, 2021 (155)
136	14KJPN	NC_000004.12 - 76436594	Oct 13, 2022 (156)
137	TopMed	NC_000004.12 - 76436594	Apr 26, 2021 (155)
138	UK 10K study - Twins	NC_000004.11 - 77357747	Oct 12, 2018 (152)
139	A Vietnamese Genetic Variation Database	NC_000004.11 - 77357747	Jul 13, 2019 (153)
140	ALFA	NC_000004.12 - 76436594	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)
rs60214442	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss85660512, ss3639249412, ss3639923505, ss3643969678	NC_000004.9:77714925:C:T	NC_000004.12:76436593:C:T	(self)
432180, ss92650710, ss108061306, ss117054561, ss163627446, ss166773548, ss198722397, ss206564608, ss277785061, ss284939147, ss293105792, ss479153993, ss1589776647, ss1712682359, ss3643444363, ss3847754288	NC_000004.10:77576770:C:T	NC_000004.12:76436593:C:T	(self)
21767703, 12100650, 8572299, 6787285, 5344943, 12713685, 4569665, 302722, 5562375, 11295083, 2990826, 24355954, 12100650, 2664937, ss221010890, ss232453481, ss239733968, ss479155586, ss479469436, ss484378168, ss536564505, ss557615357, ss651424008, ss778719356, ss782635371, ss783604918, ss831885446, ss834178736, ss980277329, ss1071661332, ss1310350219, ss1429933222, ss1580622346, ss1610397689, ss1653391722, ss1752532306, ss1801686389, ss1923520445, ss1969780408, ss2022345926, ss2095145053, ss2150474472, ss2625673664, ss2634136450, ss2705948482, ss2811041841, ss2994950792, ss3345790088, ss3628994227, ss3632071864, ss3633338785, ss3634057922, ss3634957427, ss3635740754, ss3636661113, ss3637493275, ss3638493603, ss3640664721, ss3652871023, ss3662834051, ss3731284800, ss3745257691, ss3761981839, ss3772752289, ss3784760413, ss3790212032, ss3795087382, ss3828621812, ss3837752625, ss3859278103, ss3905536291, ss3985076795, ss4017152167, ss5166386647, ss5237351412, ss5314967663, ss5507578082, ss5635345961, ss5799618378, ss5844204297, ss5963723908, ss5979704215, ss5980232670	NC_000004.11:77357746:C:T	NC_000004.12:76436593:C:T	(self)
28633075, 154194742, 2641469, 34756842, 456461131, 7072985015, ss2264098166, ss3024947653, ss3712346980, ss3805124113, ss3843190105, ss4619083575, ss5259736130, ss5458436527, ss5541107140, ss5700919738, ss5805220082, ss5854291219, ss5864047675	NC_000004.12:76436593:C:T	NC_000004.12:76436593:C:T	(self)
ss13851964, ss17791363	NT_016354.16:1852451:C:T	NC_000004.12:76436593:C:T	(self)
ss44544756, ss65804219, ss66863983, ss66933098, ss68075087, ss68902453, ss70459336, ss70979897, ss75674288, ss84888515, ss104084588, ss152539387, ss157477070, ss159850702, ss161572805, ss169494940	NT_016354.19:1905467:C:T	NC_000004.12:76436593: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 rs10006043

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

rs10006043