Name: rs55882937
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.

rs55882937

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr12:95004144-95004159 (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: del(A)₈ / del(A)₇ / delAAA / delAA…
del(A)₈ / del(A)₇ / delAAA / delAA / delA / dupA / dupAA / dupAAA
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₈=0.000004 (1/264690, TOPMED)
dupA=0.04476 (493/11014, ALFA)
dupA=0.4 (3/8, KOREAN)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NDUFA12 : 2KB Upstream 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	11014	AAAAAAAAAAAAAAAA=0.93508	AAAAAAAA=0.00000, AAAAAAAAA=0.00000, AAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAA=0.01952, AAAAAAAAAAAAAAAAA=0.04476, AAAAAAAAAAAAAAAAAA=0.00064, AAAAAAAAAAAAAAAAAAA=0.00000	0.918251	0.008175	0.073574	32
European	Sub	9048	AAAAAAAAAAAAAAAA=0.9211	AAAAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0238, AAAAAAAAAAAAAAAAA=0.0544, AAAAAAAAAAAAAAAAAA=0.0008, AAAAAAAAAAAAAAAAAAA=0.0000	0.899696	0.010054	0.09025	32
African	Sub	1024	AAAAAAAAAAAAAAAA=1.0000	AAAAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	30	AAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	994	AAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	70	AAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	50	AAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	20	AAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	80	AAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	462	AAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	56	AAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	274	AAAAAAAAAAAAAAAA=0.996	AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.004, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	0.992701	0.0	0.007299	0

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)₁₆=0.999996	del(A)₈=0.000004
Allele Frequency Aggregator	Total	Global	11014	(A)₁₆=0.93508	del(A)₈=0.00000, del(A)₇=0.00000, delAA=0.00000, delA=0.01952, dupA=0.04476, dupAA=0.00064, dupAAA=0.00000
Allele Frequency Aggregator	European	Sub	9048	(A)₁₆=0.9211	del(A)₈=0.0000, del(A)₇=0.0000, delAA=0.0000, delA=0.0238, dupA=0.0544, dupAA=0.0008, dupAAA=0.0000
Allele Frequency Aggregator	African	Sub	1024	(A)₁₆=1.0000	del(A)₈=0.0000, del(A)₇=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	462	(A)₁₆=1.000	del(A)₈=0.000, del(A)₇=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Other	Sub	274	(A)₁₆=0.996	del(A)₈=0.000, del(A)₇=0.000, delAA=0.000, delA=0.000, dupA=0.004, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	80	(A)₁₆=1.00	del(A)₈=0.00, del(A)₇=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Asian	Sub	70	(A)₁₆=1.00	del(A)₈=0.00, del(A)₇=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	South Asian	Sub	56	(A)₁₆=1.00	del(A)₈=0.00, del(A)₇=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
KOREAN population from KRGDB	KOREAN	Study-wide	8	- No frequency provided	dupA=0.4

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.95004152_95004159del
GRCh38.p14 chr 12	NC_000012.12:g.95004153_95004159del
GRCh38.p14 chr 12	NC_000012.12:g.95004157_95004159del
GRCh38.p14 chr 12	NC_000012.12:g.95004158_95004159del
GRCh38.p14 chr 12	NC_000012.12:g.95004159del
GRCh38.p14 chr 12	NC_000012.12:g.95004159dup
GRCh38.p14 chr 12	NC_000012.12:g.95004158_95004159dup
GRCh38.p14 chr 12	NC_000012.12:g.95004157_95004159dup
GRCh37.p13 chr 12	NC_000012.11:g.95397928_95397935del
GRCh37.p13 chr 12	NC_000012.11:g.95397929_95397935del
GRCh37.p13 chr 12	NC_000012.11:g.95397933_95397935del
GRCh37.p13 chr 12	NC_000012.11:g.95397934_95397935del
GRCh37.p13 chr 12	NC_000012.11:g.95397935del
GRCh37.p13 chr 12	NC_000012.11:g.95397935dup
GRCh37.p13 chr 12	NC_000012.11:g.95397934_95397935dup
GRCh37.p13 chr 12	NC_000012.11:g.95397933_95397935dup
NDUFA12 RefSeqGene	NG_032672.1:g.4563_4570del
NDUFA12 RefSeqGene	NG_032672.1:g.4564_4570del
NDUFA12 RefSeqGene	NG_032672.1:g.4568_4570del
NDUFA12 RefSeqGene	NG_032672.1:g.4569_4570del
NDUFA12 RefSeqGene	NG_032672.1:g.4570del
NDUFA12 RefSeqGene	NG_032672.1:g.4570dup
NDUFA12 RefSeqGene	NG_032672.1:g.4569_4570dup
NDUFA12 RefSeqGene	NG_032672.1:g.4568_4570dup

Gene: NDUFA12, NADH:ubiquinone oxidoreductase subunit A12 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
NDUFA12 transcript variant 2	NM_001258338.2:c.	N/A	Upstream Transcript Variant
NDUFA12 transcript variant 1	NM_018838.5:c.	N/A	Upstream Transcript 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)₁₆=	del(A)₈	del(A)₇	delAAA	delAA	delA	dupA	dupAA	dupAAA
GRCh38.p14 chr 12	NC_000012.12:g.95004144_95004159=	NC_000012.12:g.95004152_95004159del	NC_000012.12:g.95004153_95004159del	NC_000012.12:g.95004157_95004159del	NC_000012.12:g.95004158_95004159del	NC_000012.12:g.95004159del	NC_000012.12:g.95004159dup	NC_000012.12:g.95004158_95004159dup	NC_000012.12:g.95004157_95004159dup
GRCh37.p13 chr 12	NC_000012.11:g.95397920_95397935=	NC_000012.11:g.95397928_95397935del	NC_000012.11:g.95397929_95397935del	NC_000012.11:g.95397933_95397935del	NC_000012.11:g.95397934_95397935del	NC_000012.11:g.95397935del	NC_000012.11:g.95397935dup	NC_000012.11:g.95397934_95397935dup	NC_000012.11:g.95397933_95397935dup
NDUFA12 RefSeqGene	NG_032672.1:g.4555_4570=	NG_032672.1:g.4563_4570del	NG_032672.1:g.4564_4570del	NG_032672.1:g.4568_4570del	NG_032672.1:g.4569_4570del	NG_032672.1:g.4570del	NG_032672.1:g.4570dup	NG_032672.1:g.4569_4570dup	NG_032672.1:g.4568_4570dup

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#.

37 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss77939496	Dec 06, 2007 (129)
2	HGSV	ss81553551	Dec 15, 2007 (144)
3	PJP	ss294768747	Jan 10, 2018 (151)
4	EVA_DECODE	ss3694245019	Jul 13, 2019 (153)
5	EVA_DECODE	ss3694245020	Jul 13, 2019 (153)
6	EVA_DECODE	ss3694245021	Jul 13, 2019 (153)
7	EVA_DECODE	ss3694245022	Jul 13, 2019 (153)
8	ACPOP	ss3739284164	Jul 13, 2019 (153)
9	ACPOP	ss3739284165	Jul 13, 2019 (153)
10	EVA	ss3833270933	Apr 27, 2020 (154)
11	EVA	ss3840208689	Apr 27, 2020 (154)
12	EVA	ss3845696689	Apr 27, 2020 (154)
13	KRGDB	ss3927596264	Apr 27, 2020 (154)
14	KOGIC	ss3972504041	Apr 27, 2020 (154)
15	KOGIC	ss3972504042	Apr 27, 2020 (154)
16	KOGIC	ss3972504043	Apr 27, 2020 (154)
17	GNOMAD	ss4257104810	Apr 26, 2021 (155)
18	GNOMAD	ss4257104811	Apr 26, 2021 (155)
19	GNOMAD	ss4257104812	Apr 26, 2021 (155)
20	GNOMAD	ss4257104813	Apr 26, 2021 (155)
21	GNOMAD	ss4257104814	Apr 26, 2021 (155)
22	GNOMAD	ss4257104815	Apr 26, 2021 (155)
23	GNOMAD	ss4257104816	Apr 26, 2021 (155)
24	GNOMAD	ss4257104817	Apr 26, 2021 (155)
25	TOPMED	ss4928960432	Apr 26, 2021 (155)
26	TOMMO_GENOMICS	ss5207666984	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5207666985	Apr 26, 2021 (155)
28	1000G_HIGH_COVERAGE	ss5291850398	Oct 16, 2022 (156)
29	1000G_HIGH_COVERAGE	ss5291850399	Oct 16, 2022 (156)
30	1000G_HIGH_COVERAGE	ss5291850400	Oct 16, 2022 (156)
31	HUGCELL_USP	ss5486490076	Oct 16, 2022 (156)
32	HUGCELL_USP	ss5486490077	Oct 16, 2022 (156)
33	HUGCELL_USP	ss5486490078	Oct 16, 2022 (156)
34	TOMMO_GENOMICS	ss5757844025	Oct 16, 2022 (156)
35	TOMMO_GENOMICS	ss5757844026	Oct 16, 2022 (156)
36	TOMMO_GENOMICS	ss5757844028	Oct 16, 2022 (156)
37	EVA	ss5850500171	Oct 16, 2022 (156)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 416156599 (NC_000012.12:95004143::A 14323/89882) Row 416156600 (NC_000012.12:95004143::AA 200/90048) Row 416156601 (NC_000012.12:95004143::AAA 1/90078)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 416156599 (NC_000012.12:95004143::A 14323/89882) Row 416156600 (NC_000012.12:95004143::AA 200/90048) Row 416156601 (NC_000012.12:95004143::AAA 1/90078)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 416156599 (NC_000012.12:95004143::A 14323/89882) Row 416156600 (NC_000012.12:95004143::AA 200/90048) Row 416156601 (NC_000012.12:95004143::AAA 1/90078)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 416156599 (NC_000012.12:95004143::A 14323/89882) Row 416156600 (NC_000012.12:95004143::AA 200/90048) Row 416156601 (NC_000012.12:95004143::AAA 1/90078)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 416156599 (NC_000012.12:95004143::A 14323/89882) Row 416156600 (NC_000012.12:95004143::AA 200/90048) Row 416156601 (NC_000012.12:95004143::AAA 1/90078)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 416156599 (NC_000012.12:95004143::A 14323/89882) Row 416156600 (NC_000012.12:95004143::AA 200/90048) Row 416156601 (NC_000012.12:95004143::AAA 1/90078)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 416156599 (NC_000012.12:95004143::A 14323/89882) Row 416156600 (NC_000012.12:95004143::AA 200/90048) Row 416156601 (NC_000012.12:95004143::AAA 1/90078)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 416156599 (NC_000012.12:95004143::A 14323/89882) Row 416156600 (NC_000012.12:95004143::AA 200/90048) Row 416156601 (NC_000012.12:95004143::AAA 1/90078)...	-	Apr 26, 2021 (155)
46	KOREAN population from KRGDB	NC_000012.11 - 95397920	Apr 27, 2020 (154)
47	Korean Genome Project Submission ignored due to conflicting rows: Row 28882042 (NC_000012.12:95004144::A 445/1826) Row 28882043 (NC_000012.12:95004143:A: 61/1826) Row 28882044 (NC_000012.12:95004144::AA 16/1826)	-	Apr 27, 2020 (154)
48	Korean Genome Project Submission ignored due to conflicting rows: Row 28882042 (NC_000012.12:95004144::A 445/1826) Row 28882043 (NC_000012.12:95004143:A: 61/1826) Row 28882044 (NC_000012.12:95004144::AA 16/1826)	-	Apr 27, 2020 (154)
49	Korean Genome Project Submission ignored due to conflicting rows: Row 28882042 (NC_000012.12:95004144::A 445/1826) Row 28882043 (NC_000012.12:95004143:A: 61/1826) Row 28882044 (NC_000012.12:95004144::AA 16/1826)	-	Apr 27, 2020 (154)
50	Northern Sweden Submission ignored due to conflicting rows: Row 12569029 (NC_000012.11:95397919::A 92/570) Row 12569030 (NC_000012.11:95397919:A: 21/570)	-	Jul 13, 2019 (153)
51	Northern Sweden Submission ignored due to conflicting rows: Row 12569029 (NC_000012.11:95397919::A 92/570) Row 12569030 (NC_000012.11:95397919:A: 21/570)	-	Jul 13, 2019 (153)
52	8.3KJPN Submission ignored due to conflicting rows: Row 65636291 (NC_000012.11:95397919::A 2516/16748) Row 65636292 (NC_000012.11:95397919:A: 28/16748)	-	Apr 26, 2021 (155)
53	8.3KJPN Submission ignored due to conflicting rows: Row 65636291 (NC_000012.11:95397919::A 2516/16748) Row 65636292 (NC_000012.11:95397919:A: 28/16748)	-	Apr 26, 2021 (155)
54	14KJPN Submission ignored due to conflicting rows: Row 91681129 (NC_000012.12:95004143::A 4211/28256) Row 91681130 (NC_000012.12:95004143:A: 37/28256) Row 91681132 (NC_000012.12:95004143::AA 6/28256)	-	Oct 16, 2022 (156)
55	14KJPN Submission ignored due to conflicting rows: Row 91681129 (NC_000012.12:95004143::A 4211/28256) Row 91681130 (NC_000012.12:95004143:A: 37/28256) Row 91681132 (NC_000012.12:95004143::AA 6/28256)	-	Oct 16, 2022 (156)
56	14KJPN Submission ignored due to conflicting rows: Row 91681129 (NC_000012.12:95004143::A 4211/28256) Row 91681130 (NC_000012.12:95004143:A: 37/28256) Row 91681132 (NC_000012.12:95004143::AA 6/28256)	-	Oct 16, 2022 (156)
57	TopMed	NC_000012.12 - 95004144	Apr 26, 2021 (155)
58	ALFA	NC_000012.12 - 95004144	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)
rs59965120	Jul 01, 2015 (144)
rs72152237	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
144506089, ss4257104817, ss4928960432	NC_000012.12:95004143:AAAAAAAA:	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA:AAAAAAAA	(self)
1434092652	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA:AAAAAAAA	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA:AAAAAAAA	(self)
ss4257104816	NC_000012.12:95004143:AAAAAAA:	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
1434092652	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
ss4257104815	NC_000012.12:95004143:AAA:	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3694245022, ss4257104814	NC_000012.12:95004143:AA:	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
1434092652	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss81553551	NC_000012.9:93900402:A:	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3739284165, ss3833270933, ss3840208689, ss5207666985	NC_000012.11:95397919:A:	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3845696689, ss3972504042, ss4257104813, ss5291850399, ss5486490078, ss5757844026	NC_000012.12:95004143:A:	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
1434092652	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3694245021	NC_000012.12:95004144:A:	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss294768747	NC_000012.10:93922066::A	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
34773658, ss3739284164, ss3927596264, ss5207666984	NC_000012.11:95397919::A	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4257104810, ss5291850398, ss5486490076, ss5757844025, ss5850500171	NC_000012.12:95004143::A	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
1434092652	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3972504041	NC_000012.12:95004144::A	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3694245020	NC_000012.12:95004145::A	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss77939496	NT_029419.12:57541241::A	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4257104811, ss5291850400, ss5486490077, ss5757844028	NC_000012.12:95004143::AA	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
1434092652	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3972504043	NC_000012.12:95004144::AA	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3694245019	NC_000012.12:95004145::AA	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4257104812	NC_000012.12:95004143::AAA	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
1434092652	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000012.12:95004143:AAAAAAAAAAAA… NC_000012.12:95004143:AAAAAAAAAAAAAAAA: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 rs55882937

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

rs55882937