Name: rs10710882
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.

rs10710882

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr12:106592207-106592216 (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: delAA / delA / dupA / dupAA
Variation Type: Indel Insertion and Deletion
Frequency: (A)₁₀=0.401107 (106169/264690, TOPMED)
delA=0.4835 (4090/8460, ALFA)
(A)₁₀=0.3450 (1673/4849, 1000G) (+ 8 more)
(A)₁₀=0.3903 (1747/4476, Estonian)
(A)₁₀=0.4017 (1548/3854, ALSPAC)
(A)₁₀=0.3859 (1431/3708, TWINSUK)
(A)₁₀=0.1567 (287/1832, Korea1K)
(A)₁₀=0.413 (412/998, GoNL)
(A)₁₀=0.323 (194/600, NorthernSweden)
(A)₁₀=0.125 (27/216, Vietnamese)
(A)₁₀=0.47 (19/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: RFX4 : Intron Variant
LOC100287944 : 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: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	8460	AAAAAAAAAA=0.5164	AAAAAAAA=0.0000, AAAAAAAAA=0.4835, AAAAAAAAAAA=0.0001, AAAAAAAAAAAA=0.0000	0.338141	0.305037	0.356822	32
European	Sub	7592	AAAAAAAAAA=0.4694	AAAAAAAA=0.0000, AAAAAAAAA=0.5304, AAAAAAAAAAA=0.0001, AAAAAAAAAAAA=0.0000	0.272991	0.33386	0.393149	32
African	Sub	652	AAAAAAAAAA=0.948	AAAAAAAA=0.000, AAAAAAAAA=0.052, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000	0.92638	0.030675	0.042945	32
African Others	Sub	32	AAAAAAAAAA=0.94	AAAAAAAA=0.00, AAAAAAAAA=0.06, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00	0.9375	0.0625	0.0	9
African American	Sub	620	AAAAAAAAAA=0.948	AAAAAAAA=0.000, AAAAAAAAA=0.052, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000	0.925806	0.029032	0.045161	32
Asian	Sub	4	AAAAAAAAAA=0.0	AAAAAAAA=0.0, AAAAAAAAA=1.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0	0.0	1.0	0.0	N/A
East Asian	Sub	2	AAAAAAAAAA=0.0	AAAAAAAA=0.0, AAAAAAAAA=1.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0	0.0	1.0	0.0	N/A
Other Asian	Sub	2	AAAAAAAAAA=0.0	AAAAAAAA=0.0, AAAAAAAAA=1.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0	0.0	1.0	0.0	N/A
Latin American 1	Sub	8	AAAAAAAAAA=1.0	AAAAAAAA=0.0, AAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	94	AAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	14	AAAAAAAAAA=0.71	AAAAAAAA=0.00, AAAAAAAAA=0.29, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00	0.714286	0.285714	0.0	4
Other	Sub	96	AAAAAAAAAA=0.78	AAAAAAAA=0.00, AAAAAAAAA=0.22, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00	0.75	0.1875	0.0625	18

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	(A)₁₀=0.401107	delA=0.598893
Allele Frequency Aggregator	Total	Global	8460	(A)₁₀=0.5164	delAA=0.0000, delA=0.4835, dupA=0.0001, dupAA=0.0000
Allele Frequency Aggregator	European	Sub	7592	(A)₁₀=0.4694	delAA=0.0000, delA=0.5304, dupA=0.0001, dupAA=0.0000
Allele Frequency Aggregator	African	Sub	652	(A)₁₀=0.948	delAA=0.000, delA=0.052, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Other	Sub	96	(A)₁₀=0.78	delAA=0.00, delA=0.22, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Latin American 2	Sub	94	(A)₁₀=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	South Asian	Sub	14	(A)₁₀=0.71	delAA=0.00, delA=0.29, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	8	(A)₁₀=1.0	delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0
Allele Frequency Aggregator	Asian	Sub	4	(A)₁₀=0.0	delAA=0.0, delA=1.0, dupA=0.0, dupAA=0.0
1000Genomes	Global	Study-wide	4849	(A)₁₀=0.3450	delA=0.6550
1000Genomes	African	Sub	1174	(A)₁₀=0.5111	delA=0.4889
1000Genomes	East Asian	Sub	1008	(A)₁₀=0.1131	delA=0.8869
1000Genomes	Europe	Sub	1003	(A)₁₀=0.3141	delA=0.6859
1000Genomes	South Asian	Sub	977	(A)₁₀=0.400	delA=0.600
1000Genomes	American	Sub	687	(A)₁₀=0.368	delA=0.632
Genetic variation in the Estonian population	Estonian	Study-wide	4476	(A)₁₀=0.3903	delA=0.6097
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(A)₁₀=0.4017	delA=0.5983
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	(A)₁₀=0.3859	delA=0.6141
Korean Genome Project	KOREAN	Study-wide	1832	(A)₁₀=0.1567	delA=0.8433
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	(A)₁₀=0.413	delA=0.587
Northern Sweden	ACPOP	Study-wide	600	(A)₁₀=0.323	delA=0.677
A Vietnamese Genetic Variation Database	Global	Study-wide	216	(A)₁₀=0.125	delA=0.875
The Danish reference pan genome	Danish	Study-wide	40	(A)₁₀=0.47	delA=0.53

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 12	NC_000012.12:g.106592215_106592216del
GRCh38.p14 chr 12	NC_000012.12:g.106592216del
GRCh38.p14 chr 12	NC_000012.12:g.106592216dup
GRCh38.p14 chr 12	NC_000012.12:g.106592215_106592216dup
GRCh37.p13 chr 12	NC_000012.11:g.106985993_106985994del
GRCh37.p13 chr 12	NC_000012.11:g.106985994del
GRCh37.p13 chr 12	NC_000012.11:g.106985994dup
GRCh37.p13 chr 12	NC_000012.11:g.106985993_106985994dup
RFX4 RefSeqGene	NG_047074.1:g.14309_14310del
RFX4 RefSeqGene	NG_047074.1:g.14310del
RFX4 RefSeqGene	NG_047074.1:g.14310dup
RFX4 RefSeqGene	NG_047074.1:g.14309_14310dup

Gene: RFX4, regulatory factor X4 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
RFX4 transcript variant 3	NM_213594.3:c.43+8852_43+… NM_213594.3:c.43+8852_43+8853del	N/A	Intron Variant
RFX4 transcript variant 4	NM_001206691.2:c.	N/A	Genic Upstream Transcript Variant
RFX4 transcript variant 1	NM_032491.6:c.	N/A	Genic Upstream Transcript Variant

Gene: LOC100287944, uncharacterized LOC100287944 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC100287944 transcript	NR_040246.1: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	(A)₁₀=	delAA	delA	dupA	dupAA
GRCh38.p14 chr 12	NC_000012.12:g.106592207_106592216=	NC_000012.12:g.106592215_106592216del	NC_000012.12:g.106592216del	NC_000012.12:g.106592216dup	NC_000012.12:g.106592215_106592216dup
GRCh37.p13 chr 12	NC_000012.11:g.106985985_106985994=	NC_000012.11:g.106985993_106985994del	NC_000012.11:g.106985994del	NC_000012.11:g.106985994dup	NC_000012.11:g.106985993_106985994dup
RFX4 RefSeqGene	NG_047074.1:g.14301_14310=	NG_047074.1:g.14309_14310del	NG_047074.1:g.14310del	NG_047074.1:g.14310dup	NG_047074.1:g.14309_14310dup
RFX4 transcript variant 3	NM_213594.2:c.43+8844=	NM_213594.2:c.43+8852_43+8853del	NM_213594.2:c.43+8853del	NM_213594.2:c.43+8853dup	NM_213594.2:c.43+8852_43+8853dup
RFX4 transcript variant 3	NM_213594.3:c.43+8844=	NM_213594.3:c.43+8852_43+8853del	NM_213594.3:c.43+8853del	NM_213594.3:c.43+8853dup	NM_213594.3:c.43+8852_43+8853dup

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#.

73 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40150906	Mar 14, 2006 (137)
2	HGSV	ss80781368	Sep 08, 2015 (146)
3	HGSV	ss80798571	Sep 08, 2015 (146)
4	HGSV	ss80819775	Sep 08, 2015 (146)
5	HGSV	ss82307759	Sep 08, 2015 (146)
6	HUMANGENOME_JCVI	ss95606830	Dec 03, 2013 (138)
7	HUMANGENOME_JCVI	ss97275752	Dec 05, 2013 (138)
8	BGI	ss104692024	Dec 01, 2009 (131)
9	GMI	ss155497435	Dec 01, 2009 (137)
10	BL	ss256132937	May 09, 2011 (137)
11	GMI	ss287897600	May 09, 2011 (137)
12	GMI	ss289150762	May 04, 2012 (137)
13	PJP	ss294773198	May 09, 2011 (137)
14	PJP	ss294773199	May 09, 2011 (137)
15	1000GENOMES	ss327478556	May 09, 2011 (137)
16	1000GENOMES	ss327576612	May 09, 2011 (137)
17	1000GENOMES	ss328029652	May 09, 2011 (137)
18	LUNTER	ss552249974	Apr 25, 2013 (138)
19	LUNTER	ss552543088	Apr 25, 2013 (138)
20	LUNTER	ss553501820	Apr 25, 2013 (138)
21	TISHKOFF	ss554670663	Apr 25, 2013 (138)
22	SSMP	ss664087500	Apr 01, 2015 (144)
23	BILGI_BIOE	ss666583177	Apr 25, 2013 (138)
24	EVA-GONL	ss989929487	Aug 21, 2014 (142)
25	1000GENOMES	ss1372575071	Aug 21, 2014 (142)
26	1000GENOMES	ss1372575074	Aug 21, 2014 (142)
27	DDI	ss1536741692	Apr 01, 2015 (144)
28	EVA_GENOME_DK	ss1574563697	Apr 01, 2015 (144)
29	EVA_UK10K_ALSPAC	ss1707613133	Apr 01, 2015 (144)
30	EVA_UK10K_TWINSUK	ss1707613222	Apr 01, 2015 (144)
31	HAMMER_LAB	ss1807407552	Sep 08, 2015 (146)
32	GENOMED	ss1967676593	Jul 19, 2016 (147)
33	JJLAB	ss2031156284	Sep 14, 2016 (149)
34	SYSTEMSBIOZJU	ss2628181169	Nov 08, 2017 (151)
35	SWEGEN	ss3010301170	Nov 08, 2017 (151)
36	MCHAISSO	ss3063744776	Nov 08, 2017 (151)
37	MCHAISSO	ss3064574870	Nov 08, 2017 (151)
38	MCHAISSO	ss3065496194	Nov 08, 2017 (151)
39	BEROUKHIMLAB	ss3644348739	Oct 12, 2018 (152)
40	BIOINF_KMB_FNS_UNIBA	ss3645274798	Oct 12, 2018 (152)
41	URBANLAB	ss3649918161	Oct 12, 2018 (152)
42	EGCUT_WGS	ss3677599337	Jul 13, 2019 (153)
43	EVA_DECODE	ss3694406857	Jul 13, 2019 (153)
44	EVA_DECODE	ss3694406858	Jul 13, 2019 (153)
45	ACPOP	ss3739357482	Jul 13, 2019 (153)
46	PACBIO	ss3787328402	Jul 13, 2019 (153)
47	PACBIO	ss3792412584	Jul 13, 2019 (153)
48	PACBIO	ss3797295634	Jul 13, 2019 (153)
49	KHV_HUMAN_GENOMES	ss3816264913	Jul 13, 2019 (153)
50	KHV_HUMAN_GENOMES	ss3816264914	Jul 13, 2019 (153)
51	EVA	ss3833314195	Apr 27, 2020 (154)
52	EVA	ss3840229247	Apr 27, 2020 (154)
53	EVA	ss3845717673	Apr 27, 2020 (154)
54	KOGIC	ss3972662403	Apr 27, 2020 (154)
55	GNOMAD	ss4258490493	Apr 26, 2021 (155)
56	GNOMAD	ss4258490494	Apr 26, 2021 (155)
57	GNOMAD	ss4258490495	Apr 26, 2021 (155)
58	TOPMED	ss4931739309	Apr 26, 2021 (155)
59	TOMMO_GENOMICS	ss5208030052	Apr 26, 2021 (155)
60	TOMMO_GENOMICS	ss5208030053	Apr 26, 2021 (155)
61	TOMMO_GENOMICS	ss5208030054	Apr 26, 2021 (155)
62	1000G_HIGH_COVERAGE	ss5292130748	Oct 16, 2022 (156)
63	1000G_HIGH_COVERAGE	ss5292130749	Oct 16, 2022 (156)
64	HUGCELL_USP	ss5486744039	Oct 16, 2022 (156)
65	HUGCELL_USP	ss5486744040	Oct 16, 2022 (156)
66	TOMMO_GENOMICS	ss5758309434	Oct 16, 2022 (156)
67	TOMMO_GENOMICS	ss5758309435	Oct 16, 2022 (156)
68	TOMMO_GENOMICS	ss5758309436	Oct 16, 2022 (156)
69	YY_MCH	ss5813622353	Oct 16, 2022 (156)
70	EVA	ss5838473902	Oct 16, 2022 (156)
71	EVA	ss5850536234	Oct 16, 2022 (156)
72	EVA	ss5905902451	Oct 16, 2022 (156)
73	EVA	ss5945303121	Oct 16, 2022 (156)
74	1000Genomes	NC_000012.11 - 106985985	Oct 12, 2018 (152)
75	The Avon Longitudinal Study of Parents and Children	NC_000012.11 - 106985985	Oct 12, 2018 (152)
76	Genetic variation in the Estonian population	NC_000012.11 - 106985985	Oct 12, 2018 (152)
77	The Danish reference pan genome	NC_000012.11 - 106985985	Apr 27, 2020 (154)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 418466933 (NC_000012.12:106592206::A 4457/138940) Row 418466934 (NC_000012.12:106592206::AA 2/138954) Row 418466935 (NC_000012.12:106592206:A: 81721/138880)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 418466933 (NC_000012.12:106592206::A 4457/138940) Row 418466934 (NC_000012.12:106592206::AA 2/138954) Row 418466935 (NC_000012.12:106592206:A: 81721/138880)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 418466933 (NC_000012.12:106592206::A 4457/138940) Row 418466934 (NC_000012.12:106592206::AA 2/138954) Row 418466935 (NC_000012.12:106592206:A: 81721/138880)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 418466933 (NC_000012.12:106592206::A 4457/138940) Row 418466934 (NC_000012.12:106592206::AA 2/138954) Row 418466935 (NC_000012.12:106592206:A: 81721/138880)...	-	Apr 26, 2021 (155)
82	Genome of the Netherlands Release 5	NC_000012.11 - 106985985	Apr 27, 2020 (154)
83	Korean Genome Project	NC_000012.12 - 106592207	Apr 27, 2020 (154)
84	Northern Sweden	NC_000012.11 - 106985985	Jul 13, 2019 (153)
85	8.3KJPN Submission ignored due to conflicting rows: Row 65999359 (NC_000012.11:106985984:A: 14516/16760) Row 65999360 (NC_000012.11:106985984:AA: 3/16760) Row 65999361 (NC_000012.11:106985984::A 6/16760)	-	Apr 26, 2021 (155)
86	8.3KJPN Submission ignored due to conflicting rows: Row 65999359 (NC_000012.11:106985984:A: 14516/16760) Row 65999360 (NC_000012.11:106985984:AA: 3/16760) Row 65999361 (NC_000012.11:106985984::A 6/16760)	-	Apr 26, 2021 (155)
87	8.3KJPN Submission ignored due to conflicting rows: Row 65999359 (NC_000012.11:106985984:A: 14516/16760) Row 65999360 (NC_000012.11:106985984:AA: 3/16760) Row 65999361 (NC_000012.11:106985984::A 6/16760)	-	Apr 26, 2021 (155)
88	14KJPN Submission ignored due to conflicting rows: Row 92146538 (NC_000012.12:106592206:A: 24491/28258) Row 92146539 (NC_000012.12:106592206:AA: 3/28258) Row 92146540 (NC_000012.12:106592206::A 11/28258)	-	Oct 16, 2022 (156)
89	14KJPN Submission ignored due to conflicting rows: Row 92146538 (NC_000012.12:106592206:A: 24491/28258) Row 92146539 (NC_000012.12:106592206:AA: 3/28258) Row 92146540 (NC_000012.12:106592206::A 11/28258)	-	Oct 16, 2022 (156)
90	14KJPN Submission ignored due to conflicting rows: Row 92146538 (NC_000012.12:106592206:A: 24491/28258) Row 92146539 (NC_000012.12:106592206:AA: 3/28258) Row 92146540 (NC_000012.12:106592206::A 11/28258)	-	Oct 16, 2022 (156)
91	TopMed	NC_000012.12 - 106592207	Apr 26, 2021 (155)
92	UK 10K study - Twins	NC_000012.11 - 106985985	Oct 12, 2018 (152)
93	A Vietnamese Genetic Variation Database	NC_000012.11 - 106985985	Jul 13, 2019 (153)
94	ALFA	NC_000012.12 - 106592207	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)
rs11331954	May 11, 2012 (137)
rs34655879	May 11, 2012 (137)
rs60964014	May 26, 2008 (130)
rs148088290	May 04, 2012 (137)
rs369333500	May 15, 2013 (138)
rs373266350	May 13, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5208030053	NC_000012.11:106985984:AA:	NC_000012.12:106592206:AAAAAAAAAA:… NC_000012.12:106592206:AAAAAAAAAA:AAAAAAAA	(self)
ss4258490495, ss5758309435	NC_000012.12:106592206:AA:	NC_000012.12:106592206:AAAAAAAAAA:… NC_000012.12:106592206:AAAAAAAAAA:AAAAAAAA	(self)
13561685918	NC_000012.12:106592206:AAAAAAAAAA:… NC_000012.12:106592206:AAAAAAAAAA:AAAAAAAA	NC_000012.12:106592206:AAAAAAAAAA:… NC_000012.12:106592206:AAAAAAAAAA:AAAAAAAA	(self)
ss80781368, ss80798571, ss80819775, ss82307759	NC_000012.9:105488460:A:	NC_000012.12:106592206:AAAAAAAAAA:… NC_000012.12:106592206:AAAAAAAAAA:AAAAAAAAA	(self)
ss256132937, ss289150762, ss294773198, ss327478556, ss327576612, ss328029652, ss552249974, ss552543088, ss553501820	NC_000012.10:105510114:A:	NC_000012.12:106592206:AAAAAAAAAA:… NC_000012.12:106592206:AAAAAAAAAA:AAAAAAAAA	(self)
ss294773199	NC_000012.10:105510123:A:	NC_000012.12:106592206:AAAAAAAAAA:… NC_000012.12:106592206:AAAAAAAAAA:AAAAAAAAA	(self)
59328567, 32947042, 23337585, 377593, 14698868, 12642347, 32947042, 7313545, ss664087500, ss666583177, ss989929487, ss1372575071, ss1536741692, ss1574563697, ss1707613133, ss1707613222, ss1807407552, ss1967676593, ss2031156284, ss2628181169, ss3010301170, ss3644348739, ss3677599337, ss3739357482, ss3787328402, ss3792412584, ss3797295634, ss3833314195, ss3840229247, ss5208030052, ss5838473902, ss5945303121	NC_000012.11:106985984:A:	NC_000012.12:106592206:AAAAAAAAAA:… NC_000012.12:106592206:AAAAAAAAAA:AAAAAAAAA	(self)
ss554670663	NC_000012.11:106985993:A:	NC_000012.12:106592206:AAAAAAAAAA:… NC_000012.12:106592206:AAAAAAAAAA:AAAAAAAAA	(self)
29040404, 147284966, ss3063744776, ss3064574870, ss3065496194, ss3645274798, ss3649918161, ss3694406858, ss3816264913, ss3845717673, ss3972662403, ss4931739309, ss5292130748, ss5486744039, ss5758309434, ss5813622353, ss5850536234, ss5905902451	NC_000012.12:106592206:A:	NC_000012.12:106592206:AAAAAAAAAA:… NC_000012.12:106592206:AAAAAAAAAA:AAAAAAAAA	(self)
13561685918	NC_000012.12:106592206:AAAAAAAAAA:… NC_000012.12:106592206:AAAAAAAAAA:AAAAAAAAA	NC_000012.12:106592206:AAAAAAAAAA:… NC_000012.12:106592206:AAAAAAAAAA:AAAAAAAAA	(self)
ss40150906, ss155497435, ss287897600	NT_029419.12:69129290:A:	NC_000012.12:106592206:AAAAAAAAAA:… NC_000012.12:106592206:AAAAAAAAAA:AAAAAAAAA	(self)
ss104692024	NT_029419.12:69129298:A:	NC_000012.12:106592206:AAAAAAAAAA:… NC_000012.12:106592206:AAAAAAAAAA:AAAAAAAAA	(self)
ss95606830, ss97275752	NT_029419.12:69129299:A:	NC_000012.12:106592206:AAAAAAAAAA:… NC_000012.12:106592206:AAAAAAAAAA:AAAAAAAAA	(self)
ss5208030054	NC_000012.11:106985984::A	NC_000012.12:106592206:AAAAAAAAAA:… NC_000012.12:106592206:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss1372575074	NC_000012.11:106985985::A	NC_000012.12:106592206:AAAAAAAAAA:… NC_000012.12:106592206:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss4258490493, ss5292130749, ss5486744040, ss5758309436	NC_000012.12:106592206::A	NC_000012.12:106592206:AAAAAAAAAA:… NC_000012.12:106592206:AAAAAAAAAA:AAAAAAAAAAA	(self)
13561685918	NC_000012.12:106592206:AAAAAAAAAA:… NC_000012.12:106592206:AAAAAAAAAA:AAAAAAAAAAA	NC_000012.12:106592206:AAAAAAAAAA:… NC_000012.12:106592206:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss3694406857, ss3816264914	NC_000012.12:106592207::A	NC_000012.12:106592206:AAAAAAAAAA:… NC_000012.12:106592206:AAAAAAAAAA:AAAAAAAAAAA	(self)
ss4258490494	NC_000012.12:106592206::AA	NC_000012.12:106592206:AAAAAAAAAA:… NC_000012.12:106592206:AAAAAAAAAA:AAAAAAAAAAAA	(self)
13561685918	NC_000012.12:106592206:AAAAAAAAAA:… NC_000012.12:106592206:AAAAAAAAAA:AAAAAAAAAAAA	NC_000012.12:106592206:AAAAAAAAAA:… NC_000012.12:106592206:AAAAAAAAAA:AAAAAAAAAAAA	(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 rs10710882

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

rs10710882