Name: rs5831925
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.

rs5831925

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:68284375-68284386 (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: delAAA / delAA / delA / dupA / dup…
delAAA / delAA / delA / dupA / dupAA / dup(A)₄ / dup(A)₈
Variation Type: Indel Insertion and Deletion
Frequency: delA=0.4378 (2400/5482, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CNRIP1 : 3 Prime UTR Variant
LOC107985892 : 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	5482	AAAAAAAAAAAA=0.4969	AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.4378, AAAAAAAAAAAAA=0.0651, AAAAAAAAA=0.0002, AAAAAAAAAAAAAA=0.0000	0.353137	0.275031	0.371832	32
European	Sub	5216	AAAAAAAAAAAA=0.4724	AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.4590, AAAAAAAAAAAAA=0.0684, AAAAAAAAA=0.0002, AAAAAAAAAAAAAA=0.0000	0.317062	0.290237	0.3927	32
African	Sub	152	AAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	4	AAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
African American	Sub	148	AAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	6	AAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	6	AAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	AAAAAAAAAAAA=0	AAAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAA=0, AAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	8	AAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	60	AAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	6	AAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other	Sub	34	AAAAAAAAAAAA=0.82	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.18, AAAAAAAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00	0.764706	0.117647	0.117647	4

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	5482	(A)₁₂=0.4969	delAAA=0.0002, delAA=0.0000, delA=0.4378, dupA=0.0651, dupAA=0.0000
Allele Frequency Aggregator	European	Sub	5216	(A)₁₂=0.4724	delAAA=0.0002, delAA=0.0000, delA=0.4590, dupA=0.0684, dupAA=0.0000
Allele Frequency Aggregator	African	Sub	152	(A)₁₂=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Latin American 2	Sub	60	(A)₁₂=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Other	Sub	34	(A)₁₂=0.82	delAAA=0.00, delAA=0.00, delA=0.18, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	8	(A)₁₂=1.0	delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0
Allele Frequency Aggregator	South Asian	Sub	6	(A)₁₂=1.0	delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0
Allele Frequency Aggregator	Asian	Sub	6	(A)₁₂=1.0	delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0

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 2	NC_000002.12:g.68284384_68284386del
GRCh38.p14 chr 2	NC_000002.12:g.68284385_68284386del
GRCh38.p14 chr 2	NC_000002.12:g.68284386del
GRCh38.p14 chr 2	NC_000002.12:g.68284386dup
GRCh38.p14 chr 2	NC_000002.12:g.68284385_68284386dup
GRCh38.p14 chr 2	NC_000002.12:g.68284383_68284386dup
GRCh38.p14 chr 2	NC_000002.12:g.68284379_68284386dup
GRCh37.p13 chr 2	NC_000002.11:g.68511516_68511518del
GRCh37.p13 chr 2	NC_000002.11:g.68511517_68511518del
GRCh37.p13 chr 2	NC_000002.11:g.68511518del
GRCh37.p13 chr 2	NC_000002.11:g.68511518dup
GRCh37.p13 chr 2	NC_000002.11:g.68511517_68511518dup
GRCh37.p13 chr 2	NC_000002.11:g.68511515_68511518dup
GRCh37.p13 chr 2	NC_000002.11:g.68511511_68511518dup

Gene: CNRIP1, cannabinoid receptor interacting protein 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CNRIP1 transcript variant 2	NM_001111101.2:c.42_53=	N/A	3 Prime UTR Variant
CNRIP1 transcript variant 3	NM_001371604.1:c.	N/A	Genic Downstream Transcript Variant
CNRIP1 transcript variant 4	NM_001371605.1:c.	N/A	Genic Downstream Transcript Variant
CNRIP1 transcript variant 5	NM_001371606.1:c.	N/A	Genic Downstream Transcript Variant
CNRIP1 transcript variant 6	NM_001371607.1:c.	N/A	Genic Downstream Transcript Variant
CNRIP1 transcript variant 7	NM_001371608.1:c.	N/A	Genic Downstream Transcript Variant
CNRIP1 transcript variant 1	NM_015463.3:c.	N/A	Genic Downstream Transcript Variant
CNRIP1 transcript variant 8	NR_163969.1:n.	N/A	Genic Downstream Transcript Variant
CNRIP1 transcript variant 9	NR_163970.1:n.	N/A	Genic Downstream Transcript Variant
CNRIP1 transcript variant 10	NR_163971.1:n.	N/A	Genic Downstream Transcript Variant

Gene: LOC107985892, uncharacterized LOC107985892 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC107985892 transcript variant X2	XR_001739526.2:n.	N/A	Intron Variant
LOC107985892 transcript variant X1	XR_001739527.2: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)₁₂=	delAAA	delAA	delA	dupA	dupAA	dup(A)₄	dup(A)₈
GRCh38.p14 chr 2	NC_000002.12:g.68284375_68284386=	NC_000002.12:g.68284384_68284386del	NC_000002.12:g.68284385_68284386del	NC_000002.12:g.68284386del	NC_000002.12:g.68284386dup	NC_000002.12:g.68284385_68284386dup	NC_000002.12:g.68284383_68284386dup	NC_000002.12:g.68284379_68284386dup
GRCh37.p13 chr 2	NC_000002.11:g.68511507_68511518=	NC_000002.11:g.68511516_68511518del	NC_000002.11:g.68511517_68511518del	NC_000002.11:g.68511518del	NC_000002.11:g.68511518dup	NC_000002.11:g.68511517_68511518dup	NC_000002.11:g.68511515_68511518dup	NC_000002.11:g.68511511_68511518dup
CNRIP1 transcript variant 2	NM_001111101.2:c.42_53=	NM_001111101.2:c.51_53del	NM_001111101.2:c.52_53del	NM_001111101.2:c.*53del	NM_001111101.2:c.*53dup	NM_001111101.2:c.52_53dup	NM_001111101.2:c.50_53dup	NM_001111101.2:c.46_53dup
CNRIP1 transcript variant CRIP1b	NM_001111101.1:c.42_53=	NM_001111101.1:c.51_53del	NM_001111101.1:c.52_53del	NM_001111101.1:c.*53del	NM_001111101.1:c.*53dup	NM_001111101.1:c.52_53dup	NM_001111101.1:c.50_53dup	NM_001111101.1:c.46_53dup

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#.

61 SubSNP, 15 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	DEVINE_LAB	ss8094996	Mar 15, 2016 (147)
2	HUMANGENOME_JCVI	ss95275755	Feb 03, 2009 (130)
3	BCMHGSC_JDW	ss103627634	Dec 06, 2013 (138)
4	BGI	ss104723140	Feb 13, 2009 (137)
5	BGI	ss105490909	Feb 13, 2009 (137)
6	BUSHMAN	ss193544638	Jul 04, 2010 (132)
7	BL	ss255929672	May 09, 2011 (137)
8	GMI	ss287699889	May 09, 2011 (137)
9	GMI	ss288175698	May 04, 2012 (137)
10	PJP	ss294988549	May 09, 2011 (137)
11	PJP	ss294988550	May 09, 2011 (134)
12	SSMP	ss663322776	Apr 01, 2015 (144)
13	BILGI_BIOE	ss666151894	Apr 25, 2013 (138)
14	DDI	ss1536292566	Apr 01, 2015 (144)
15	HAMMER_LAB	ss1796899705	Sep 08, 2015 (146)
16	HAMMER_LAB	ss1796899708	Sep 08, 2015 (146)
17	TMC_SNPDB	ss1997120577	Jul 19, 2016 (147)
18	SWEGEN	ss2989687118	Nov 08, 2017 (151)
19	MCHAISSO	ss3064791773	Nov 08, 2017 (151)
20	BEROUKHIMLAB	ss3644093894	Oct 11, 2018 (152)
21	BIOINF_KMB_FNS_UNIBA	ss3645558399	Oct 11, 2018 (152)
22	URBANLAB	ss3647056977	Oct 11, 2018 (152)
23	EVA_DECODE	ss3704114204	Jul 13, 2019 (153)
24	EVA_DECODE	ss3704114205	Jul 13, 2019 (153)
25	EVA_DECODE	ss3704114206	Jul 13, 2019 (153)
26	EVA_DECODE	ss3704114207	Jul 13, 2019 (153)
27	ACPOP	ss3728529491	Jul 13, 2019 (153)
28	ACPOP	ss3728529492	Jul 13, 2019 (153)
29	PACBIO	ss3783891345	Jul 13, 2019 (153)
30	PACBIO	ss3789473685	Jul 13, 2019 (153)
31	PACBIO	ss3794346628	Jul 13, 2019 (153)
32	EVA	ss3827036906	Apr 25, 2020 (154)
33	EVA	ss3836928082	Apr 25, 2020 (154)
34	EVA	ss3842344043	Apr 25, 2020 (154)
35	FSA-LAB	ss3984178180	Apr 26, 2021 (155)
36	FSA-LAB	ss3984178181	Apr 26, 2021 (155)
37	GNOMAD	ss4043287650	Apr 26, 2021 (155)
38	GNOMAD	ss4043287651	Apr 26, 2021 (155)
39	GNOMAD	ss4043287652	Apr 26, 2021 (155)
40	GNOMAD	ss4043287653	Apr 26, 2021 (155)
41	GNOMAD	ss4043287654	Apr 26, 2021 (155)
42	GNOMAD	ss4043287655	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5151878284	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5151878285	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5151878286	Apr 26, 2021 (155)
46	EVA	ss5237169648	Apr 26, 2021 (155)
47	EVA	ss5237169649	Apr 26, 2021 (155)
48	1000G_HIGH_COVERAGE	ss5248452767	Oct 12, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5248452768	Oct 12, 2022 (156)
50	1000G_HIGH_COVERAGE	ss5248452769	Oct 12, 2022 (156)
51	HUGCELL_USP	ss5448620209	Oct 12, 2022 (156)
52	HUGCELL_USP	ss5448620210	Oct 12, 2022 (156)
53	EVA	ss5624099904	Oct 12, 2022 (156)
54	EVA	ss5624099905	Oct 12, 2022 (156)
55	TOMMO_GENOMICS	ss5680650051	Oct 12, 2022 (156)
56	TOMMO_GENOMICS	ss5680650052	Oct 12, 2022 (156)
57	TOMMO_GENOMICS	ss5680650053	Oct 12, 2022 (156)
58	EVA	ss5800095164	Oct 12, 2022 (156)
59	EVA	ss5820249886	Oct 12, 2022 (156)
60	EVA	ss5980061495	Oct 12, 2022 (156)
61	EVA	ss5981205212	Oct 12, 2022 (156)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 61506876 (NC_000002.12:68284374::A 21268/137134) Row 61506877 (NC_000002.12:68284374::AA 36/137262) Row 61506878 (NC_000002.12:68284374::AAAA 1/137272)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 61506876 (NC_000002.12:68284374::A 21268/137134) Row 61506877 (NC_000002.12:68284374::AA 36/137262) Row 61506878 (NC_000002.12:68284374::AAAA 1/137272)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 61506876 (NC_000002.12:68284374::A 21268/137134) Row 61506877 (NC_000002.12:68284374::AA 36/137262) Row 61506878 (NC_000002.12:68284374::AAAA 1/137272)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 61506876 (NC_000002.12:68284374::A 21268/137134) Row 61506877 (NC_000002.12:68284374::AA 36/137262) Row 61506878 (NC_000002.12:68284374::AAAA 1/137272)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 61506876 (NC_000002.12:68284374::A 21268/137134) Row 61506877 (NC_000002.12:68284374::AA 36/137262) Row 61506878 (NC_000002.12:68284374::AAAA 1/137272)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 61506876 (NC_000002.12:68284374::A 21268/137134) Row 61506877 (NC_000002.12:68284374::AA 36/137262) Row 61506878 (NC_000002.12:68284374::AAAA 1/137272)...	-	Apr 26, 2021 (155)
68	Northern Sweden Submission ignored due to conflicting rows: Row 1814356 (NC_000002.11:68511506:A: 363/600) Row 1814357 (NC_000002.11:68511506::A 39/600)	-	Jul 13, 2019 (153)
69	Northern Sweden Submission ignored due to conflicting rows: Row 1814356 (NC_000002.11:68511506:A: 363/600) Row 1814357 (NC_000002.11:68511506::A 39/600)	-	Jul 13, 2019 (153)
70	8.3KJPN Submission ignored due to conflicting rows: Row 9847591 (NC_000002.11:68511506:A: 9308/16756) Row 9847592 (NC_000002.11:68511506::A 3089/16756) Row 9847593 (NC_000002.11:68511506::AA 3/16756)	-	Apr 26, 2021 (155)
71	8.3KJPN Submission ignored due to conflicting rows: Row 9847591 (NC_000002.11:68511506:A: 9308/16756) Row 9847592 (NC_000002.11:68511506::A 3089/16756) Row 9847593 (NC_000002.11:68511506::AA 3/16756)	-	Apr 26, 2021 (155)
72	8.3KJPN Submission ignored due to conflicting rows: Row 9847591 (NC_000002.11:68511506:A: 9308/16756) Row 9847592 (NC_000002.11:68511506::A 3089/16756) Row 9847593 (NC_000002.11:68511506::AA 3/16756)	-	Apr 26, 2021 (155)
73	14KJPN Submission ignored due to conflicting rows: Row 14487155 (NC_000002.12:68284374:A: 15743/28258) Row 14487156 (NC_000002.12:68284374::A 5225/28258) Row 14487157 (NC_000002.12:68284374::AA 6/28258)	-	Oct 12, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 14487155 (NC_000002.12:68284374:A: 15743/28258) Row 14487156 (NC_000002.12:68284374::A 5225/28258) Row 14487157 (NC_000002.12:68284374::AA 6/28258)	-	Oct 12, 2022 (156)
75	14KJPN Submission ignored due to conflicting rows: Row 14487155 (NC_000002.12:68284374:A: 15743/28258) Row 14487156 (NC_000002.12:68284374::A 5225/28258) Row 14487157 (NC_000002.12:68284374::AA 6/28258)	-	Oct 12, 2022 (156)
76	ALFA	NC_000002.12 - 68284375	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)
rs33980752	May 23, 2006 (127)
rs72540704	May 11, 2012 (137)
rs72591033	Feb 26, 2009 (130)
rs138927971	May 11, 2012 (137)
rs149098232	May 04, 2012 (137)
rs368293529	May 13, 2013 (138)
rs74263923	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
11795787064	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAA	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAA	(self)
ss3984178181	NC_000002.11:68511506:AA:	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAAA	(self)
ss3704114207, ss4043287655, ss5248452769	NC_000002.12:68284374:AA:	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAAA	(self)
11795787064	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAAA	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAAA	(self)
ss103627634	NT_022184.15:47333403:AA:	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAAA	(self)
ss255929672, ss288175698, ss294988549	NC_000002.10:68365010:A:	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss294988550	NC_000002.10:68365021:A:	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss663322776, ss666151894, ss1536292566, ss1796899708, ss2989687118, ss3644093894, ss3728529491, ss3783891345, ss3789473685, ss3794346628, ss3827036906, ss3836928082, ss5151878284, ss5624099905, ss5800095164, ss5820249886, ss5980061495, ss5981205212	NC_000002.11:68511506:A:	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss3064791773, ss3645558399, ss3647056977, ss3842344043, ss4043287654, ss5237169648, ss5248452768, ss5448620209, ss5680650051	NC_000002.12:68284374:A:	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAAAA	(self)
11795787064	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAAAA	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss3704114206	NC_000002.12:68284375:A:	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss287699889	NT_022184.15:47333393:A:	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss104723140, ss105490909	NT_022184.15:47333403:A:	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss8094996, ss95275755	NT_022184.15:47333404:A:	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss1796899705, ss3728529492, ss3984178180, ss5151878285, ss5624099904	NC_000002.11:68511506::A	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss1997120577	NC_000002.11:68511507::A	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4043287650, ss5248452767, ss5448620210, ss5680650052	NC_000002.12:68284374::A	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
11795787064	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss5237169649	NC_000002.12:68284375::A	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3704114205	NC_000002.12:68284376::A	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss193544638	NT_022184.16:52138255::A	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss5151878286	NC_000002.11:68511506::AA	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4043287651, ss5680650053	NC_000002.12:68284374::AA	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
11795787064	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3704114204	NC_000002.12:68284376::AA	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4043287652	NC_000002.12:68284374::AAAA	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4043287653	NC_000002.12:68284374::AAAAAAAA	NC_000002.12:68284374:AAAAAAAAAAAA… NC_000002.12:68284374:AAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(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 rs5831925

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

rs5831925