Name: rs371040471
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.

rs371040471

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:184936022-184936036 (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 / dupA…
delAA / delA / dupA / dupAA / dupAAA / dup(A)₄
Variation Type: Indel Insertion and Deletion
Frequency: delAA=0.0000 (0/7884, ALFA)
delA=0.0000 (0/7884, ALFA)
dupA=0.0000 (0/7884, ALFA) (+ 2 more)
dupAA=0.0000 (0/7884, ALFA)
dupAAA=0.0000 (0/7884, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NIBAN1 : Intron Variant
LOC124904469 : Non Coding Transcript 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	HWEP
Total	Global	7884	AAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	5108	AAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	1840	AAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African Others	Sub	66	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	1774	AAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
Asian	Sub	56	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	40	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	16	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	98	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	402	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	56	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	324	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	1.0	N/A

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	7884	(A)₁₅=1.0000	delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	European	Sub	5108	(A)₁₅=1.0000	delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	African	Sub	1840	(A)₁₅=1.0000	delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	402	(A)₁₅=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Other	Sub	324	(A)₁₅=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	98	(A)₁₅=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	South Asian	Sub	56	(A)₁₅=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Asian	Sub	56	(A)₁₅=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00

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.184936035_184936036del
GRCh38.p14 chr 1	NC_000001.11:g.184936036del
GRCh38.p14 chr 1	NC_000001.11:g.184936036dup
GRCh38.p14 chr 1	NC_000001.11:g.184936035_184936036dup
GRCh38.p14 chr 1	NC_000001.11:g.184936034_184936036dup
GRCh38.p14 chr 1	NC_000001.11:g.184936033_184936036dup
GRCh37.p13 chr 1	NC_000001.10:g.184905167_184905168del
GRCh37.p13 chr 1	NC_000001.10:g.184905168del
GRCh37.p13 chr 1	NC_000001.10:g.184905168dup
GRCh37.p13 chr 1	NC_000001.10:g.184905167_184905168dup
GRCh37.p13 chr 1	NC_000001.10:g.184905166_184905168dup
GRCh37.p13 chr 1	NC_000001.10:g.184905165_184905168dup
NIBAN1 RefSeqGene	NG_051588.1:g.43564_43565del
NIBAN1 RefSeqGene	NG_051588.1:g.43565del
NIBAN1 RefSeqGene	NG_051588.1:g.43565dup
NIBAN1 RefSeqGene	NG_051588.1:g.43564_43565dup
NIBAN1 RefSeqGene	NG_051588.1:g.43563_43565dup
NIBAN1 RefSeqGene	NG_051588.1:g.43562_43565dup

Gene: NIBAN1, niban apoptosis regulator 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NIBAN1 transcript	NM_052966.4:c.56-36714_56… NM_052966.4:c.56-36714_56-36713del	N/A	Intron Variant
NIBAN1 transcript variant X1	XM_047444091.1:c.232+2833… XM_047444091.1:c.232+28330_232+28331del	N/A	Intron Variant
NIBAN1 transcript variant X2	XM_047444093.1:c.232+2833… XM_047444093.1:c.232+28330_232+28331del	N/A	Intron Variant
NIBAN1 transcript variant X3	XM_047444094.1:c.232+2833… XM_047444094.1:c.232+28330_232+28331del	N/A	Intron Variant
NIBAN1 transcript variant X4	XM_047444098.1:c.56-36714… XM_047444098.1:c.56-36714_56-36713del	N/A	Intron Variant
NIBAN1 transcript variant X5	XM_047444102.1:c.56-36714… XM_047444102.1:c.56-36714_56-36713del	N/A	Intron Variant

Gene: LOC124904469, uncharacterized LOC124904469 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC124904469 transcript variant X1	XR_007066770.1:n.7628_762… XR_007066770.1:n.7628_7629del	N/A	Non Coding Transcript Variant
LOC124904469 transcript variant X1	XR_007066770.1:n.7629del	N/A	Non Coding Transcript Variant
LOC124904469 transcript variant X1	XR_007066770.1:n.7629dup	N/A	Non Coding Transcript Variant
LOC124904469 transcript variant X1	XR_007066770.1:n.7628_762… XR_007066770.1:n.7628_7629dup	N/A	Non Coding Transcript Variant
LOC124904469 transcript variant X1	XR_007066770.1:n.7627_762… XR_007066770.1:n.7627_7629dup	N/A	Non Coding Transcript Variant
LOC124904469 transcript variant X1	XR_007066770.1:n.7626_762… XR_007066770.1:n.7626_7629dup	N/A	Non Coding 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)₁₅=	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄
GRCh38.p14 chr 1	NC_000001.11:g.184936022_184936036=	NC_000001.11:g.184936035_184936036del	NC_000001.11:g.184936036del	NC_000001.11:g.184936036dup	NC_000001.11:g.184936035_184936036dup	NC_000001.11:g.184936034_184936036dup	NC_000001.11:g.184936033_184936036dup
GRCh37.p13 chr 1	NC_000001.10:g.184905154_184905168=	NC_000001.10:g.184905167_184905168del	NC_000001.10:g.184905168del	NC_000001.10:g.184905168dup	NC_000001.10:g.184905167_184905168dup	NC_000001.10:g.184905166_184905168dup	NC_000001.10:g.184905165_184905168dup
NIBAN1 RefSeqGene	NG_051588.1:g.43551_43565=	NG_051588.1:g.43564_43565del	NG_051588.1:g.43565del	NG_051588.1:g.43565dup	NG_051588.1:g.43564_43565dup	NG_051588.1:g.43563_43565dup	NG_051588.1:g.43562_43565dup
LOC124904469 transcript variant X1	XR_007066770.1:n.7615_7629=	XR_007066770.1:n.7628_7629del	XR_007066770.1:n.7629del	XR_007066770.1:n.7629dup	XR_007066770.1:n.7628_7629dup	XR_007066770.1:n.7627_7629dup	XR_007066770.1:n.7626_7629dup
FAM129A transcript	NM_052966.3:c.56-36712=	NM_052966.3:c.56-36713_56-36712del	NM_052966.3:c.56-36712del	NM_052966.3:c.56-36712dup	NM_052966.3:c.56-36713_56-36712dup	NM_052966.3:c.56-36714_56-36712dup	NM_052966.3:c.56-36715_56-36712dup
NIBAN1 transcript	NM_052966.4:c.56-36713=	NM_052966.4:c.56-36714_56-36713del	NM_052966.4:c.56-36713del	NM_052966.4:c.56-36713dup	NM_052966.4:c.56-36714_56-36713dup	NM_052966.4:c.56-36715_56-36713dup	NM_052966.4:c.56-36716_56-36713dup
FAM129A transcript variant X1	XM_005244873.1:c.56-36712=	XM_005244873.1:c.56-36713_56-36712del	XM_005244873.1:c.56-36712del	XM_005244873.1:c.56-36712dup	XM_005244873.1:c.56-36713_56-36712dup	XM_005244873.1:c.56-36714_56-36712dup	XM_005244873.1:c.56-36715_56-36712dup
NIBAN1 transcript variant X1	XM_047444091.1:c.232+28331=	XM_047444091.1:c.232+28330_232+28331del	XM_047444091.1:c.232+28331del	XM_047444091.1:c.232+28331dup	XM_047444091.1:c.232+28330_232+28331dup	XM_047444091.1:c.232+28329_232+28331dup	XM_047444091.1:c.232+28328_232+28331dup
NIBAN1 transcript variant X2	XM_047444093.1:c.232+28331=	XM_047444093.1:c.232+28330_232+28331del	XM_047444093.1:c.232+28331del	XM_047444093.1:c.232+28331dup	XM_047444093.1:c.232+28330_232+28331dup	XM_047444093.1:c.232+28329_232+28331dup	XM_047444093.1:c.232+28328_232+28331dup
NIBAN1 transcript variant X3	XM_047444094.1:c.232+28331=	XM_047444094.1:c.232+28330_232+28331del	XM_047444094.1:c.232+28331del	XM_047444094.1:c.232+28331dup	XM_047444094.1:c.232+28330_232+28331dup	XM_047444094.1:c.232+28329_232+28331dup	XM_047444094.1:c.232+28328_232+28331dup
NIBAN1 transcript variant X4	XM_047444098.1:c.56-36713=	XM_047444098.1:c.56-36714_56-36713del	XM_047444098.1:c.56-36713del	XM_047444098.1:c.56-36713dup	XM_047444098.1:c.56-36714_56-36713dup	XM_047444098.1:c.56-36715_56-36713dup	XM_047444098.1:c.56-36716_56-36713dup
NIBAN1 transcript variant X5	XM_047444102.1:c.56-36713=	XM_047444102.1:c.56-36714_56-36713del	XM_047444102.1:c.56-36713del	XM_047444102.1:c.56-36713dup	XM_047444102.1:c.56-36714_56-36713dup	XM_047444102.1:c.56-36715_56-36713dup	XM_047444102.1:c.56-36716_56-36713dup

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#.

34 SubSNP, 12 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SSMP	ss663138890	Apr 01, 2015 (144)
2	BILGI_BIOE	ss666118964	Apr 25, 2013 (138)
3	HAMMER_LAB	ss1795399397	Sep 08, 2015 (146)
4	SWEGEN	ss2988088177	Nov 08, 2017 (151)
5	SWEGEN	ss2988088178	Nov 08, 2017 (151)
6	MCHAISSO	ss3065338998	Nov 08, 2017 (151)
7	EVA_DECODE	ss3688190175	Jul 12, 2019 (153)
8	EVA_DECODE	ss3688190176	Jul 12, 2019 (153)
9	EVA_DECODE	ss3688190177	Jul 12, 2019 (153)
10	EVA_DECODE	ss3688190178	Jul 12, 2019 (153)
11	PACBIO	ss3783626986	Jul 12, 2019 (153)
12	PACBIO	ss3789248646	Jul 12, 2019 (153)
13	PACBIO	ss3794120797	Jul 12, 2019 (153)
14	EVA	ss3826532654	Apr 25, 2020 (154)
15	EVA	ss3836662658	Apr 25, 2020 (154)
16	EVA	ss3842073057	Apr 25, 2020 (154)
17	GNOMAD	ss4007347696	Apr 25, 2021 (155)
18	GNOMAD	ss4007347697	Apr 25, 2021 (155)
19	GNOMAD	ss4007347698	Apr 25, 2021 (155)
20	GNOMAD	ss4007347700	Apr 25, 2021 (155)
21	TOMMO_GENOMICS	ss5147425086	Apr 25, 2021 (155)
22	TOMMO_GENOMICS	ss5147425087	Apr 25, 2021 (155)
23	TOMMO_GENOMICS	ss5147425088	Apr 25, 2021 (155)
24	1000G_HIGH_COVERAGE	ss5245017614	Oct 12, 2022 (156)
25	1000G_HIGH_COVERAGE	ss5245017615	Oct 12, 2022 (156)
26	1000G_HIGH_COVERAGE	ss5245017616	Oct 12, 2022 (156)
27	1000G_HIGH_COVERAGE	ss5245017617	Oct 12, 2022 (156)
28	HUGCELL_USP	ss5445530717	Oct 12, 2022 (156)
29	HUGCELL_USP	ss5445530718	Oct 12, 2022 (156)
30	HUGCELL_USP	ss5445530719	Oct 12, 2022 (156)
31	TOMMO_GENOMICS	ss5674896075	Oct 12, 2022 (156)
32	TOMMO_GENOMICS	ss5674896076	Oct 12, 2022 (156)
33	TOMMO_GENOMICS	ss5674896077	Oct 12, 2022 (156)
34	EVA	ss5980003084	Oct 12, 2022 (156)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33084947 (NC_000001.11:184936021::A 23515/114178) Row 33084948 (NC_000001.11:184936021::AA 653/114436) Row 33084949 (NC_000001.11:184936021::AAA 4/114486)...	-	Apr 25, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33084947 (NC_000001.11:184936021::A 23515/114178) Row 33084948 (NC_000001.11:184936021::AA 653/114436) Row 33084949 (NC_000001.11:184936021::AAA 4/114486)...	-	Apr 25, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33084947 (NC_000001.11:184936021::A 23515/114178) Row 33084948 (NC_000001.11:184936021::AA 653/114436) Row 33084949 (NC_000001.11:184936021::AAA 4/114486)...	-	Apr 25, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33084947 (NC_000001.11:184936021::A 23515/114178) Row 33084948 (NC_000001.11:184936021::AA 653/114436) Row 33084949 (NC_000001.11:184936021::AAA 4/114486)...	-	Apr 25, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33084947 (NC_000001.11:184936021::A 23515/114178) Row 33084948 (NC_000001.11:184936021::AA 653/114436) Row 33084949 (NC_000001.11:184936021::AAA 4/114486)...	-	Apr 25, 2021 (155)
40	8.3KJPN Submission ignored due to conflicting rows: Row 5394393 (NC_000001.10:184905153::A 5144/16740) Row 5394394 (NC_000001.10:184905153::AA 152/16740) Row 5394395 (NC_000001.10:184905153:A: 16/16740)	-	Apr 25, 2021 (155)
41	8.3KJPN Submission ignored due to conflicting rows: Row 5394393 (NC_000001.10:184905153::A 5144/16740) Row 5394394 (NC_000001.10:184905153::AA 152/16740) Row 5394395 (NC_000001.10:184905153:A: 16/16740)	-	Apr 25, 2021 (155)
42	8.3KJPN Submission ignored due to conflicting rows: Row 5394393 (NC_000001.10:184905153::A 5144/16740) Row 5394394 (NC_000001.10:184905153::AA 152/16740) Row 5394395 (NC_000001.10:184905153:A: 16/16740)	-	Apr 25, 2021 (155)
43	14KJPN Submission ignored due to conflicting rows: Row 8733179 (NC_000001.11:184936021::AA 297/28256) Row 8733180 (NC_000001.11:184936021::A 8761/28256) Row 8733181 (NC_000001.11:184936021:A: 27/28256)	-	Oct 12, 2022 (156)
44	14KJPN Submission ignored due to conflicting rows: Row 8733179 (NC_000001.11:184936021::AA 297/28256) Row 8733180 (NC_000001.11:184936021::A 8761/28256) Row 8733181 (NC_000001.11:184936021:A: 27/28256)	-	Oct 12, 2022 (156)
45	14KJPN Submission ignored due to conflicting rows: Row 8733179 (NC_000001.11:184936021::AA 297/28256) Row 8733180 (NC_000001.11:184936021::A 8761/28256) Row 8733181 (NC_000001.11:184936021:A: 27/28256)	-	Oct 12, 2022 (156)
46	ALFA	NC_000001.11 - 184936022	Apr 25, 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)
rs373157229	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3688190178, ss4007347700	NC_000001.11:184936021:AA:	NC_000001.11:184936021:AAAAAAAAAAA… NC_000001.11:184936021:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
5981144546	NC_000001.11:184936021:AAAAAAAAAAA… NC_000001.11:184936021:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000001.11:184936021:AAAAAAAAAAA… NC_000001.11:184936021:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss1795399397, ss5147425088	NC_000001.10:184905153:A:	NC_000001.11:184936021:AAAAAAAAAAA… NC_000001.11:184936021:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss5245017615, ss5445530719, ss5674896077	NC_000001.11:184936021:A:	NC_000001.11:184936021:AAAAAAAAAAA… NC_000001.11:184936021:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
5981144546	NC_000001.11:184936021:AAAAAAAAAAA… NC_000001.11:184936021:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000001.11:184936021:AAAAAAAAAAA… NC_000001.11:184936021:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3688190177	NC_000001.11:184936022:A:	NC_000001.11:184936021:AAAAAAAAAAA… NC_000001.11:184936021:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss663138890, ss666118964, ss2988088177, ss3783626986, ss3789248646, ss3794120797, ss3826532654, ss5147425086	NC_000001.10:184905153::A	NC_000001.11:184936021:AAAAAAAAAAA… NC_000001.11:184936021:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3065338998, ss4007347696, ss5245017614, ss5445530717, ss5674896076	NC_000001.11:184936021::A	NC_000001.11:184936021:AAAAAAAAAAA… NC_000001.11:184936021:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
5981144546	NC_000001.11:184936021:AAAAAAAAAAA… NC_000001.11:184936021:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000001.11:184936021:AAAAAAAAAAA… NC_000001.11:184936021:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3688190176	NC_000001.11:184936023::A	NC_000001.11:184936021:AAAAAAAAAAA… NC_000001.11:184936021:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss2988088178, ss3836662658, ss5147425087	NC_000001.10:184905153::AA	NC_000001.11:184936021:AAAAAAAAAAA… NC_000001.11:184936021:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3842073057, ss4007347697, ss5245017616, ss5445530718, ss5674896075	NC_000001.11:184936021::AA	NC_000001.11:184936021:AAAAAAAAAAA… NC_000001.11:184936021:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
5981144546	NC_000001.11:184936021:AAAAAAAAAAA… NC_000001.11:184936021:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000001.11:184936021:AAAAAAAAAAA… NC_000001.11:184936021:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3688190175	NC_000001.11:184936023::AA	NC_000001.11:184936021:AAAAAAAAAAA… NC_000001.11:184936021:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4007347698, ss5245017617	NC_000001.11:184936021::AAA	NC_000001.11:184936021:AAAAAAAAAAA… NC_000001.11:184936021:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
5981144546	NC_000001.11:184936021:AAAAAAAAAAA… NC_000001.11:184936021:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000001.11:184936021:AAAAAAAAAAA… NC_000001.11:184936021:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss5980003084	NC_000001.10:184905153::AAAA	NC_000001.11:184936021:AAAAAAAAAAA… NC_000001.11:184936021:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs371040471

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

rs371040471