Name: rs796413997
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.

rs796413997

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr15:64689661-64689677 (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)₅ / del(A)₄ / delAAA / delAA…
del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₅=0.0000 (0/6768, ALFA)
del(A)₄=0.0000 (0/6768, ALFA)
delAAA=0.0000 (0/6768, ALFA) (+ 4 more)
delAA=0.0000 (0/6768, ALFA)
delA=0.0000 (0/6768, ALFA)
dupA=0.0000 (0/6768, ALFA)
dupAA=0.0000 (0/6768, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: OAZ2 : 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	HWEP
Total	Global	6768	AAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	4568	AAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	1238	AAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African Others	Sub	50	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	1188	AAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
Asian	Sub	104	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
East Asian	Sub	80	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	24	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	72	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	440	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	74	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	272	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=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	6768	(A)₁₇=1.0000	del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	European	Sub	4568	(A)₁₇=1.0000	del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	African	Sub	1238	(A)₁₇=1.0000	del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	440	(A)₁₇=1.000	del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Other	Sub	272	(A)₁₇=1.000	del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Asian	Sub	104	(A)₁₇=1.000	del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	South Asian	Sub	74	(A)₁₇=1.00	del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	72	(A)₁₇=1.00	del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=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 15	NC_000015.10:g.64689673_64689677del
GRCh38.p14 chr 15	NC_000015.10:g.64689674_64689677del
GRCh38.p14 chr 15	NC_000015.10:g.64689675_64689677del
GRCh38.p14 chr 15	NC_000015.10:g.64689676_64689677del
GRCh38.p14 chr 15	NC_000015.10:g.64689677del
GRCh38.p14 chr 15	NC_000015.10:g.64689677dup
GRCh38.p14 chr 15	NC_000015.10:g.64689676_64689677dup
GRCh38.p14 chr 15	NC_000015.10:g.64689675_64689677dup
GRCh38.p14 chr 15	NC_000015.10:g.64689674_64689677dup
GRCh38.p14 chr 15	NC_000015.10:g.64689673_64689677dup
GRCh37.p13 chr 15	NC_000015.9:g.64981872_64981876del
GRCh37.p13 chr 15	NC_000015.9:g.64981873_64981876del
GRCh37.p13 chr 15	NC_000015.9:g.64981874_64981876del
GRCh37.p13 chr 15	NC_000015.9:g.64981875_64981876del
GRCh37.p13 chr 15	NC_000015.9:g.64981876del
GRCh37.p13 chr 15	NC_000015.9:g.64981876dup
GRCh37.p13 chr 15	NC_000015.9:g.64981875_64981876dup
GRCh37.p13 chr 15	NC_000015.9:g.64981874_64981876dup
GRCh37.p13 chr 15	NC_000015.9:g.64981873_64981876dup
GRCh37.p13 chr 15	NC_000015.9:g.64981872_64981876dup

Gene: OAZ2, ornithine decarboxylase antizyme 2 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
OAZ2 transcript variant 2	NM_001301302.1:c.351-496_… NM_001301302.1:c.351-496_351-492del	N/A	Intron Variant
OAZ2 transcript variant 1	NM_002537.3:c.354-496_354… NM_002537.3:c.354-496_354-492del	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)₁₇=	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅
GRCh38.p14 chr 15	NC_000015.10:g.64689661_64689677=	NC_000015.10:g.64689673_64689677del	NC_000015.10:g.64689674_64689677del	NC_000015.10:g.64689675_64689677del	NC_000015.10:g.64689676_64689677del	NC_000015.10:g.64689677del	NC_000015.10:g.64689677dup	NC_000015.10:g.64689676_64689677dup	NC_000015.10:g.64689675_64689677dup	NC_000015.10:g.64689674_64689677dup	NC_000015.10:g.64689673_64689677dup
GRCh37.p13 chr 15	NC_000015.9:g.64981860_64981876=	NC_000015.9:g.64981872_64981876del	NC_000015.9:g.64981873_64981876del	NC_000015.9:g.64981874_64981876del	NC_000015.9:g.64981875_64981876del	NC_000015.9:g.64981876del	NC_000015.9:g.64981876dup	NC_000015.9:g.64981875_64981876dup	NC_000015.9:g.64981874_64981876dup	NC_000015.9:g.64981873_64981876dup	NC_000015.9:g.64981872_64981876dup
OAZ2 transcript variant 2	NM_001301302.1:c.351-492=	NM_001301302.1:c.351-496_351-492del	NM_001301302.1:c.351-495_351-492del	NM_001301302.1:c.351-494_351-492del	NM_001301302.1:c.351-493_351-492del	NM_001301302.1:c.351-492del	NM_001301302.1:c.351-492dup	NM_001301302.1:c.351-493_351-492dup	NM_001301302.1:c.351-494_351-492dup	NM_001301302.1:c.351-495_351-492dup	NM_001301302.1:c.351-496_351-492dup
OAZ2 transcript	NM_002537.2:c.354-492=	NM_002537.2:c.354-496_354-492del	NM_002537.2:c.354-495_354-492del	NM_002537.2:c.354-494_354-492del	NM_002537.2:c.354-493_354-492del	NM_002537.2:c.354-492del	NM_002537.2:c.354-492dup	NM_002537.2:c.354-493_354-492dup	NM_002537.2:c.354-494_354-492dup	NM_002537.2:c.354-495_354-492dup	NM_002537.2:c.354-496_354-492dup
OAZ2 transcript variant 1	NM_002537.3:c.354-492=	NM_002537.3:c.354-496_354-492del	NM_002537.3:c.354-495_354-492del	NM_002537.3:c.354-494_354-492del	NM_002537.3:c.354-493_354-492del	NM_002537.3:c.354-492del	NM_002537.3:c.354-492dup	NM_002537.3:c.354-493_354-492dup	NM_002537.3:c.354-494_354-492dup	NM_002537.3:c.354-495_354-492dup	NM_002537.3:c.354-496_354-492dup

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#.

30 SubSNP, 15 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	PADH-LAB_SPU	ss1751349650	Sep 08, 2015 (146)
2	HAMMER_LAB	ss1808247842	Sep 08, 2015 (146)
3	SWEGEN	ss3013438619	Nov 08, 2017 (151)
4	MCHAISSO	ss3064660039	Nov 08, 2017 (151)
5	MCHAISSO	ss3065592162	Nov 08, 2017 (151)
6	EVA	ss3834284358	Apr 27, 2020 (154)
7	EVA	ss3840741282	Apr 27, 2020 (154)
8	EVA	ss3846230516	Apr 27, 2020 (154)
9	GNOMAD	ss4290465177	Apr 27, 2021 (155)
10	GNOMAD	ss4290465178	Apr 27, 2021 (155)
11	GNOMAD	ss4290465179	Apr 27, 2021 (155)
12	GNOMAD	ss4290465180	Apr 27, 2021 (155)
13	GNOMAD	ss4290465181	Apr 27, 2021 (155)
14	GNOMAD	ss4290465182	Apr 27, 2021 (155)
15	GNOMAD	ss4290465183	Apr 27, 2021 (155)
16	GNOMAD	ss4290465184	Apr 27, 2021 (155)
17	GNOMAD	ss4290465185	Apr 27, 2021 (155)
18	GNOMAD	ss4290465186	Apr 27, 2021 (155)
19	TOMMO_GENOMICS	ss5216639452	Apr 27, 2021 (155)
20	TOMMO_GENOMICS	ss5216639453	Apr 27, 2021 (155)
21	1000G_HIGH_COVERAGE	ss5298779950	Oct 16, 2022 (156)
22	1000G_HIGH_COVERAGE	ss5298779951	Oct 16, 2022 (156)
23	1000G_HIGH_COVERAGE	ss5298779952	Oct 16, 2022 (156)
24	1000G_HIGH_COVERAGE	ss5298779953	Oct 16, 2022 (156)
25	HUGCELL_USP	ss5492476216	Oct 16, 2022 (156)
26	HUGCELL_USP	ss5492476217	Oct 16, 2022 (156)
27	HUGCELL_USP	ss5492476218	Oct 16, 2022 (156)
28	HUGCELL_USP	ss5492476219	Oct 16, 2022 (156)
29	TOMMO_GENOMICS	ss5770575101	Oct 16, 2022 (156)
30	TOMMO_GENOMICS	ss5770575102	Oct 16, 2022 (156)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 471901883 (NC_000015.10:64689660::A 12955/104486) Row 471901884 (NC_000015.10:64689660::AA 54/104626) Row 471901885 (NC_000015.10:64689660::AAA 2/104642)...	-	Apr 27, 2021 (155)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 471901883 (NC_000015.10:64689660::A 12955/104486) Row 471901884 (NC_000015.10:64689660::AA 54/104626) Row 471901885 (NC_000015.10:64689660::AAA 2/104642)...	-	Apr 27, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 471901883 (NC_000015.10:64689660::A 12955/104486) Row 471901884 (NC_000015.10:64689660::AA 54/104626) Row 471901885 (NC_000015.10:64689660::AAA 2/104642)...	-	Apr 27, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 471901883 (NC_000015.10:64689660::A 12955/104486) Row 471901884 (NC_000015.10:64689660::AA 54/104626) Row 471901885 (NC_000015.10:64689660::AAA 2/104642)...	-	Apr 27, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 471901883 (NC_000015.10:64689660::A 12955/104486) Row 471901884 (NC_000015.10:64689660::AA 54/104626) Row 471901885 (NC_000015.10:64689660::AAA 2/104642)...	-	Apr 27, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 471901883 (NC_000015.10:64689660::A 12955/104486) Row 471901884 (NC_000015.10:64689660::AA 54/104626) Row 471901885 (NC_000015.10:64689660::AAA 2/104642)...	-	Apr 27, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 471901883 (NC_000015.10:64689660::A 12955/104486) Row 471901884 (NC_000015.10:64689660::AA 54/104626) Row 471901885 (NC_000015.10:64689660::AAA 2/104642)...	-	Apr 27, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 471901883 (NC_000015.10:64689660::A 12955/104486) Row 471901884 (NC_000015.10:64689660::AA 54/104626) Row 471901885 (NC_000015.10:64689660::AAA 2/104642)...	-	Apr 27, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 471901883 (NC_000015.10:64689660::A 12955/104486) Row 471901884 (NC_000015.10:64689660::AA 54/104626) Row 471901885 (NC_000015.10:64689660::AAA 2/104642)...	-	Apr 27, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 471901883 (NC_000015.10:64689660::A 12955/104486) Row 471901884 (NC_000015.10:64689660::AA 54/104626) Row 471901885 (NC_000015.10:64689660::AAA 2/104642)...	-	Apr 27, 2021 (155)
41	8.3KJPN Submission ignored due to conflicting rows: Row 74608759 (NC_000015.9:64981859::A 53/16758) Row 74608760 (NC_000015.9:64981859:A: 43/16758)	-	Apr 27, 2021 (155)
42	8.3KJPN Submission ignored due to conflicting rows: Row 74608759 (NC_000015.9:64981859::A 53/16758) Row 74608760 (NC_000015.9:64981859:A: 43/16758)	-	Apr 27, 2021 (155)
43	14KJPN Submission ignored due to conflicting rows: Row 104412205 (NC_000015.10:64689660::A 74/28254) Row 104412206 (NC_000015.10:64689660:A: 70/28254)	-	Oct 16, 2022 (156)
44	14KJPN Submission ignored due to conflicting rows: Row 104412205 (NC_000015.10:64689660::A 74/28254) Row 104412206 (NC_000015.10:64689660:A: 70/28254)	-	Oct 16, 2022 (156)
45	ALFA	NC_000015.10 - 64689661	Apr 27, 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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4290465186, ss5298779952, ss5492476219	NC_000015.10:64689660:AAAAA:	NC_000015.10:64689660:AAAAAAAAAAAA… NC_000015.10:64689660:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
22899605	NC_000015.10:64689660:AAAAAAAAAAAA… NC_000015.10:64689660:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000015.10:64689660:AAAAAAAAAAAA… NC_000015.10:64689660:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4290465185	NC_000015.10:64689660:AAAA:	NC_000015.10:64689660:AAAAAAAAAAAA… NC_000015.10:64689660:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
22899605	NC_000015.10:64689660:AAAAAAAAAAAA… NC_000015.10:64689660:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000015.10:64689660:AAAAAAAAAAAA… NC_000015.10:64689660:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4290465184	NC_000015.10:64689660:AAA:	NC_000015.10:64689660:AAAAAAAAAAAA… NC_000015.10:64689660:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
22899605	NC_000015.10:64689660:AAAAAAAAAAAA… NC_000015.10:64689660:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000015.10:64689660:AAAAAAAAAAAA… NC_000015.10:64689660:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4290465183, ss5298779953, ss5492476218	NC_000015.10:64689660:AA:	NC_000015.10:64689660:AAAAAAAAAAAA… NC_000015.10:64689660:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
22899605	NC_000015.10:64689660:AAAAAAAAAAAA… NC_000015.10:64689660:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000015.10:64689660:AAAAAAAAAAAA… NC_000015.10:64689660:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss1751349650, ss1808247842, ss3013438619, ss3840741282, ss5216639453	NC_000015.9:64981859:A:	NC_000015.10:64689660:AAAAAAAAAAAA… NC_000015.10:64689660:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3064660039, ss3065592162, ss3846230516, ss4290465182, ss5298779950, ss5492476216, ss5770575102	NC_000015.10:64689660:A:	NC_000015.10:64689660:AAAAAAAAAAAA… NC_000015.10:64689660:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
22899605	NC_000015.10:64689660:AAAAAAAAAAAA… NC_000015.10:64689660:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000015.10:64689660:AAAAAAAAAAAA… NC_000015.10:64689660:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3834284358, ss5216639452	NC_000015.9:64981859::A	NC_000015.10:64689660:AAAAAAAAAAAA… NC_000015.10:64689660:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4290465177, ss5298779951, ss5492476217, ss5770575101	NC_000015.10:64689660::A	NC_000015.10:64689660:AAAAAAAAAAAA… NC_000015.10:64689660:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
22899605	NC_000015.10:64689660:AAAAAAAAAAAA… NC_000015.10:64689660:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000015.10:64689660:AAAAAAAAAAAA… NC_000015.10:64689660:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4290465178	NC_000015.10:64689660::AA	NC_000015.10:64689660:AAAAAAAAAAAA… NC_000015.10:64689660:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
22899605	NC_000015.10:64689660:AAAAAAAAAAAA… NC_000015.10:64689660:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000015.10:64689660:AAAAAAAAAAAA… NC_000015.10:64689660:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4290465179	NC_000015.10:64689660::AAA	NC_000015.10:64689660:AAAAAAAAAAAA… NC_000015.10:64689660:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4290465180	NC_000015.10:64689660::AAAA	NC_000015.10:64689660:AAAAAAAAAAAA… NC_000015.10:64689660:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4290465181	NC_000015.10:64689660::AAAAA	NC_000015.10:64689660:AAAAAAAAAAAA… NC_000015.10:64689660:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(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 rs796413997

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

rs796413997