Name: rs67946703
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.

rs67946703

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr12:94990272-94990283 (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 / dup(…
delAA / delA / dupA / dupAA / dup(A)₇
Variation Type: Indel Insertion and Deletion
Frequency: delA=0.2675 (1555/5812, ALFA)
(A)₁₂=0.4073 (2040/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NDUFA12 : 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	5812	AAAAAAAAAAAA=0.4666	AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.2675, AAAAAAAAAAAAA=0.2653, AAAAAAAAAAAAAA=0.0005, AAAAAAAAAAAAAAAAAAA=0.0000	0.550118	0.196344	0.253538	32
European	Sub	5086	AAAAAAAAAAAA=0.3913	AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.3053, AAAAAAAAAAAAA=0.3028, AAAAAAAAAAAAAA=0.0006, AAAAAAAAAAAAAAAAAAA=0.0000	0.429213	0.248689	0.322097	32
African	Sub	602	AAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	24	AAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	578	AAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	4	AAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	2	AAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	2	AAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	18	AAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	18	AAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	14	AAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	70	AAAAAAAAAAAA=0.94	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.03, AAAAAAAAAAAAA=0.03, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	0.969697	0.030303	0.0	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
Allele Frequency Aggregator	Total	Global	5812	(A)₁₂=0.4666	delAA=0.0000, delA=0.2675, dupA=0.2653, dupAA=0.0005, dup(A)₇=0.0000
Allele Frequency Aggregator	European	Sub	5086	(A)₁₂=0.3913	delAA=0.0000, delA=0.3053, dupA=0.3028, dupAA=0.0006, dup(A)₇=0.0000
Allele Frequency Aggregator	African	Sub	602	(A)₁₂=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dup(A)₇=0.000
Allele Frequency Aggregator	Other	Sub	70	(A)₁₂=0.94	delAA=0.00, delA=0.03, dupA=0.03, dupAA=0.00, dup(A)₇=0.00
Allele Frequency Aggregator	Latin American 1	Sub	18	(A)₁₂=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dup(A)₇=0.00
Allele Frequency Aggregator	Latin American 2	Sub	18	(A)₁₂=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dup(A)₇=0.00
Allele Frequency Aggregator	South Asian	Sub	14	(A)₁₂=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dup(A)₇=0.00
Allele Frequency Aggregator	Asian	Sub	4	(A)₁₂=1.0	delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dup(A)₇=0.0
1000Genomes	Global	Study-wide	5008	(A)₁₂=0.4073	delA=0.5927
1000Genomes	African	Sub	1322	(A)₁₂=0.3616	delA=0.6384
1000Genomes	East Asian	Sub	1008	(A)₁₂=0.4802	delA=0.5198
1000Genomes	Europe	Sub	1006	(A)₁₂=0.4175	delA=0.5825
1000Genomes	South Asian	Sub	978	(A)₁₂=0.421	delA=0.579
1000Genomes	American	Sub	694	(A)₁₂=0.354	delA=0.646

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.94990282_94990283del
GRCh38.p14 chr 12	NC_000012.12:g.94990283del
GRCh38.p14 chr 12	NC_000012.12:g.94990283dup
GRCh38.p14 chr 12	NC_000012.12:g.94990282_94990283dup
GRCh38.p14 chr 12	NC_000012.12:g.94990277_94990283dup
GRCh37.p13 chr 12	NC_000012.11:g.95384058_95384059del
GRCh37.p13 chr 12	NC_000012.11:g.95384059del
GRCh37.p13 chr 12	NC_000012.11:g.95384059dup
GRCh37.p13 chr 12	NC_000012.11:g.95384058_95384059dup
GRCh37.p13 chr 12	NC_000012.11:g.95384053_95384059dup
NDUFA12 RefSeqGene	NG_032672.1:g.18441_18442del
NDUFA12 RefSeqGene	NG_032672.1:g.18442del
NDUFA12 RefSeqGene	NG_032672.1:g.18442dup
NDUFA12 RefSeqGene	NG_032672.1:g.18441_18442dup
NDUFA12 RefSeqGene	NG_032672.1:g.18436_18442dup

Gene: NDUFA12, NADH:ubiquinone oxidoreductase subunit A12 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NDUFA12 transcript variant 2	NM_001258338.2:c.169+1246… NM_001258338.2:c.169+12466_169+12467del	N/A	Intron Variant
NDUFA12 transcript variant 1	NM_018838.5:c.257+3897_25… NM_018838.5:c.257+3897_257+3898del	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)₁₂=	delAA	delA	dupA	dupAA	dup(A)₇
GRCh38.p14 chr 12	NC_000012.12:g.94990272_94990283=	NC_000012.12:g.94990282_94990283del	NC_000012.12:g.94990283del	NC_000012.12:g.94990283dup	NC_000012.12:g.94990282_94990283dup	NC_000012.12:g.94990277_94990283dup
GRCh37.p13 chr 12	NC_000012.11:g.95384048_95384059=	NC_000012.11:g.95384058_95384059del	NC_000012.11:g.95384059del	NC_000012.11:g.95384059dup	NC_000012.11:g.95384058_95384059dup	NC_000012.11:g.95384053_95384059dup
NDUFA12 RefSeqGene	NG_032672.1:g.18431_18442=	NG_032672.1:g.18441_18442del	NG_032672.1:g.18442del	NG_032672.1:g.18442dup	NG_032672.1:g.18441_18442dup	NG_032672.1:g.18436_18442dup
NDUFA12 transcript variant 2	NM_001258338.1:c.169+12467=	NM_001258338.1:c.169+12466_169+12467del	NM_001258338.1:c.169+12467del	NM_001258338.1:c.169+12467dup	NM_001258338.1:c.169+12466_169+12467dup	NM_001258338.1:c.169+12461_169+12467dup
NDUFA12 transcript variant 2	NM_001258338.2:c.169+12467=	NM_001258338.2:c.169+12466_169+12467del	NM_001258338.2:c.169+12467del	NM_001258338.2:c.169+12467dup	NM_001258338.2:c.169+12466_169+12467dup	NM_001258338.2:c.169+12461_169+12467dup
NDUFA12 transcript variant 1	NM_018838.4:c.257+3898=	NM_018838.4:c.257+3897_257+3898del	NM_018838.4:c.257+3898del	NM_018838.4:c.257+3898dup	NM_018838.4:c.257+3897_257+3898dup	NM_018838.4:c.257+3892_257+3898dup
NDUFA12 transcript variant 1	NM_018838.5:c.257+3898=	NM_018838.5:c.257+3897_257+3898del	NM_018838.5:c.257+3898del	NM_018838.5:c.257+3898dup	NM_018838.5:c.257+3897_257+3898dup	NM_018838.5:c.257+3892_257+3898dup

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#.

49 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95604728	Feb 06, 2009 (130)
2	GMI	ss289145860	May 04, 2012 (137)
3	GMI	ss289145861	Oct 12, 2018 (152)
4	PJP	ss294768737	May 09, 2011 (134)
5	TISHKOFF	ss554665229	Apr 25, 2013 (138)
6	BILGI_BIOE	ss666580305	Apr 25, 2013 (138)
7	1000GENOMES	ss1372473217	Aug 21, 2014 (142)
8	DDI	ss1536738538	Apr 01, 2015 (144)
9	EVA_UK10K_ALSPAC	ss1707580359	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1707580437	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1710573999	Apr 01, 2015 (144)
12	EVA_UK10K_ALSPAC	ss1710574012	Apr 01, 2015 (144)
13	SWEGEN	ss3010169154	Nov 08, 2017 (151)
14	MCHAISSO	ss3063741545	Nov 08, 2017 (151)
15	MCHAISSO	ss3064571450	Nov 08, 2017 (151)
16	BIOINF_KMB_FNS_UNIBA	ss3645270000	Oct 12, 2018 (152)
17	EVA_DECODE	ss3694244808	Jul 13, 2019 (153)
18	EVA_DECODE	ss3694244809	Jul 13, 2019 (153)
19	EVA_DECODE	ss3694244811	Jul 13, 2019 (153)
20	EVA_DECODE	ss3694244812	Jul 13, 2019 (153)
21	ACPOP	ss3739284047	Jul 13, 2019 (153)
22	ACPOP	ss3739284048	Jul 13, 2019 (153)
23	PACBIO	ss3787305768	Jul 13, 2019 (153)
24	PACBIO	ss3792393796	Jul 13, 2019 (153)
25	PACBIO	ss3797276781	Jul 13, 2019 (153)
26	KHV_HUMAN_GENOMES	ss3816166451	Jul 13, 2019 (153)
27	EVA	ss3833270862	Apr 27, 2020 (154)
28	EVA	ss3845696642	Apr 27, 2020 (154)
29	KOGIC	ss3972503761	Apr 27, 2020 (154)
30	KOGIC	ss3972503762	Apr 27, 2020 (154)
31	KOGIC	ss3972503763	Apr 27, 2020 (154)
32	GNOMAD	ss4257103115	Apr 26, 2021 (155)
33	GNOMAD	ss4257103116	Apr 26, 2021 (155)
34	GNOMAD	ss4257103117	Apr 26, 2021 (155)
35	GNOMAD	ss4257103118	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5207666473	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5207666474	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5207666475	Apr 26, 2021 (155)
39	1000G_HIGH_COVERAGE	ss5291850033	Oct 16, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5291850034	Oct 16, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5291850035	Oct 16, 2022 (156)
42	HUGCELL_USP	ss5486489747	Oct 16, 2022 (156)
43	HUGCELL_USP	ss5486489748	Oct 16, 2022 (156)
44	HUGCELL_USP	ss5486489749	Oct 16, 2022 (156)
45	TOMMO_GENOMICS	ss5757843351	Oct 16, 2022 (156)
46	TOMMO_GENOMICS	ss5757843352	Oct 16, 2022 (156)
47	TOMMO_GENOMICS	ss5757843353	Oct 16, 2022 (156)
48	EVA	ss5838363823	Oct 16, 2022 (156)
49	EVA	ss5838363824	Oct 16, 2022 (156)
50	1000Genomes	NC_000012.11 - 95384048	Oct 12, 2018 (152)
51	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 32754094 (NC_000012.11:95384047::A 1511/3854) Row 32754095 (NC_000012.11:95384047:A: 1407/3854)	-	Oct 12, 2018 (152)
52	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 32754094 (NC_000012.11:95384047::A 1511/3854) Row 32754095 (NC_000012.11:95384047:A: 1407/3854)	-	Oct 12, 2018 (152)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 416153780 (NC_000012.12:94990271::A 43521/134536) Row 416153781 (NC_000012.12:94990271::AA 70/134668) Row 416153782 (NC_000012.12:94990271::AAAAAAA 7/134736)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 416153780 (NC_000012.12:94990271::A 43521/134536) Row 416153781 (NC_000012.12:94990271::AA 70/134668) Row 416153782 (NC_000012.12:94990271::AAAAAAA 7/134736)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 416153780 (NC_000012.12:94990271::A 43521/134536) Row 416153781 (NC_000012.12:94990271::AA 70/134668) Row 416153782 (NC_000012.12:94990271::AAAAAAA 7/134736)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 416153780 (NC_000012.12:94990271::A 43521/134536) Row 416153781 (NC_000012.12:94990271::AA 70/134668) Row 416153782 (NC_000012.12:94990271::AAAAAAA 7/134736)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 416153780 (NC_000012.12:94990271::A 43521/134536) Row 416153781 (NC_000012.12:94990271::AA 70/134668) Row 416153782 (NC_000012.12:94990271::AAAAAAA 7/134736)...	-	Apr 26, 2021 (155)
58	Korean Genome Project Submission ignored due to conflicting rows: Row 28881762 (NC_000012.12:94990272::A 704/1830) Row 28881763 (NC_000012.12:94990271:A: 787/1830) Row 28881764 (NC_000012.12:94990272::AA 21/1830)	-	Apr 27, 2020 (154)
59	Korean Genome Project Submission ignored due to conflicting rows: Row 28881762 (NC_000012.12:94990272::A 704/1830) Row 28881763 (NC_000012.12:94990271:A: 787/1830) Row 28881764 (NC_000012.12:94990272::AA 21/1830)	-	Apr 27, 2020 (154)
60	Korean Genome Project Submission ignored due to conflicting rows: Row 28881762 (NC_000012.12:94990272::A 704/1830) Row 28881763 (NC_000012.12:94990271:A: 787/1830) Row 28881764 (NC_000012.12:94990272::AA 21/1830)	-	Apr 27, 2020 (154)
61	Northern Sweden Submission ignored due to conflicting rows: Row 12568912 (NC_000012.11:95384047::A 170/580) Row 12568913 (NC_000012.11:95384047:A: 236/580)	-	Jul 13, 2019 (153)
62	Northern Sweden Submission ignored due to conflicting rows: Row 12568912 (NC_000012.11:95384047::A 170/580) Row 12568913 (NC_000012.11:95384047:A: 236/580)	-	Jul 13, 2019 (153)
63	8.3KJPN Submission ignored due to conflicting rows: Row 65635780 (NC_000012.11:95384047:A: 7754/16754) Row 65635781 (NC_000012.11:95384047::A 7020/16754) Row 65635782 (NC_000012.11:95384047::AA 5/16754)	-	Apr 26, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 65635780 (NC_000012.11:95384047:A: 7754/16754) Row 65635781 (NC_000012.11:95384047::A 7020/16754) Row 65635782 (NC_000012.11:95384047::AA 5/16754)	-	Apr 26, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 65635780 (NC_000012.11:95384047:A: 7754/16754) Row 65635781 (NC_000012.11:95384047::A 7020/16754) Row 65635782 (NC_000012.11:95384047::AA 5/16754)	-	Apr 26, 2021 (155)
66	14KJPN Submission ignored due to conflicting rows: Row 91680455 (NC_000012.12:94990271:A: 13106/28242) Row 91680456 (NC_000012.12:94990271::A 11697/28242) Row 91680457 (NC_000012.12:94990271::AA 6/28242)	-	Oct 16, 2022 (156)
67	14KJPN Submission ignored due to conflicting rows: Row 91680455 (NC_000012.12:94990271:A: 13106/28242) Row 91680456 (NC_000012.12:94990271::A 11697/28242) Row 91680457 (NC_000012.12:94990271::AA 6/28242)	-	Oct 16, 2022 (156)
68	14KJPN Submission ignored due to conflicting rows: Row 91680455 (NC_000012.12:94990271:A: 13106/28242) Row 91680456 (NC_000012.12:94990271::A 11697/28242) Row 91680457 (NC_000012.12:94990271::AA 6/28242)	-	Oct 16, 2022 (156)
69	UK 10K study - Twins Submission ignored due to conflicting rows: Row 32754094 (NC_000012.11:95384047::A 1517/3708) Row 32754095 (NC_000012.11:95384047:A: 1316/3708)	-	Oct 12, 2018 (152)
70	UK 10K study - Twins Submission ignored due to conflicting rows: Row 32754094 (NC_000012.11:95384047::A 1517/3708) Row 32754095 (NC_000012.11:95384047:A: 1316/3708)	-	Oct 12, 2018 (152)
71	ALFA	NC_000012.12 - 94990272	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)
rs67946704	Feb 27, 2009 (130)
rs67951443	Feb 27, 2009 (130)
rs200013472	May 11, 2012 (137)
rs372605858	May 13, 2013 (138)
rs375296961	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4257103118	NC_000012.12:94990271:AA:	NC_000012.12:94990271:AAAAAAAAAAAA… NC_000012.12:94990271:AAAAAAAAAAAA:AAAAAAAAAA	(self)
6116150178	NC_000012.12:94990271:AAAAAAAAAAAA… NC_000012.12:94990271:AAAAAAAAAAAA:AAAAAAAAAA	NC_000012.12:94990271:AAAAAAAAAAAA… NC_000012.12:94990271:AAAAAAAAAAAA:AAAAAAAAAA	(self)
ss289145860	NC_000012.10:93908178:A:	NC_000012.12:94990271:AAAAAAAAAAAA… NC_000012.12:94990271:AAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss294768737	NC_000012.10:93908189:A:	NC_000012.12:94990271:AAAAAAAAAAAA… NC_000012.12:94990271:AAAAAAAAAAAA:AAAAAAAAAAA	(self)
58996849, ss666580305, ss1372473217, ss1707580359, ss1707580437, ss3010169154, ss3739284048, ss3787305768, ss3792393796, ss3797276781, ss3833270862, ss5207666473, ss5838363824	NC_000012.11:95384047:A:	NC_000012.12:94990271:AAAAAAAAAAAA… NC_000012.12:94990271:AAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss554665229	NC_000012.11:95384058:A:	NC_000012.12:94990271:AAAAAAAAAAAA… NC_000012.12:94990271:AAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss3063741545, ss3064571450, ss3645270000, ss3694244811, ss3816166451, ss3972503762, ss5291850033, ss5486489747, ss5757843351	NC_000012.12:94990271:A:	NC_000012.12:94990271:AAAAAAAAAAAA… NC_000012.12:94990271:AAAAAAAAAAAA:AAAAAAAAAAA	(self)
6116150178	NC_000012.12:94990271:AAAAAAAAAAAA… NC_000012.12:94990271:AAAAAAAAAAAA:AAAAAAAAAAA	NC_000012.12:94990271:AAAAAAAAAAAA… NC_000012.12:94990271:AAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss95604728	NT_029419.12:57527364:A:	NC_000012.12:94990271:AAAAAAAAAAAA… NC_000012.12:94990271:AAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss289145861	NC_000012.10:93908190::A	NC_000012.12:94990271:AAAAAAAAAAAA… NC_000012.12:94990271:AAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss1536738538, ss3739284047, ss5207666474, ss5838363823	NC_000012.11:95384047::A	NC_000012.12:94990271:AAAAAAAAAAAA… NC_000012.12:94990271:AAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss1710573999, ss1710574012	NC_000012.11:95384048::A	NC_000012.12:94990271:AAAAAAAAAAAA… NC_000012.12:94990271:AAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3845696642, ss4257103115, ss5291850034, ss5486489748, ss5757843352	NC_000012.12:94990271::A	NC_000012.12:94990271:AAAAAAAAAAAA… NC_000012.12:94990271:AAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
6116150178	NC_000012.12:94990271:AAAAAAAAAAAA… NC_000012.12:94990271:AAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000012.12:94990271:AAAAAAAAAAAA… NC_000012.12:94990271:AAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3694244809, ss3972503761	NC_000012.12:94990272::A	NC_000012.12:94990271:AAAAAAAAAAAA… NC_000012.12:94990271:AAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3694244812	NC_000012.12:94990278::A	NC_000012.12:94990271:AAAAAAAAAAAA… NC_000012.12:94990271:AAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss5207666475	NC_000012.11:95384047::AA	NC_000012.12:94990271:AAAAAAAAAAAA… NC_000012.12:94990271:AAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4257103116, ss5291850035, ss5486489749, ss5757843353	NC_000012.12:94990271::AA	NC_000012.12:94990271:AAAAAAAAAAAA… NC_000012.12:94990271:AAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
6116150178	NC_000012.12:94990271:AAAAAAAAAAAA… NC_000012.12:94990271:AAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000012.12:94990271:AAAAAAAAAAAA… NC_000012.12:94990271:AAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3694244808, ss3972503763	NC_000012.12:94990272::AA	NC_000012.12:94990271:AAAAAAAAAAAA… NC_000012.12:94990271:AAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4257103117	NC_000012.12:94990271::AAAAAAA	NC_000012.12:94990271:AAAAAAAAAAAA… NC_000012.12:94990271:AAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
6116150178	NC_000012.12:94990271:AAAAAAAAAAAA… NC_000012.12:94990271:AAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000012.12:94990271:AAAAAAAAAAAA… NC_000012.12:94990271:AAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(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 rs67946703

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

rs67946703