Name: rs11372823
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.

rs11372823

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr12:113092327-113092339 (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
Variation Type: Indel Insertion and Deletion
Frequency: (A)₁₃=0.3470 (1738/5008, 1000G)
delAA=0.000 (0/400, ALFA)
delA=0.000 (0/400, ALFA) (+ 2 more)
dupA=0.000 (0/400, ALFA)
dupAA=0.000 (0/400, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: DTX1 : 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	400	AAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
European	Sub	328	AAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African	Sub	26	AAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African Others	Sub	0	AAAAAAAAAAAAA=0	AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0	0	0	0	N/A
African American	Sub	26	AAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Asian	Sub	8	AAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	4	AAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	4	AAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	4	AAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	14	AAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	4	AAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other	Sub	16	AAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupA=0.6530
1000Genomes	African	Sub	1322	- No frequency provided	dupA=0.7133
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupA=0.6528
1000Genomes	Europe	Sub	1006	- No frequency provided	dupA=0.5845
1000Genomes	South Asian	Sub	978	- No frequency provided	dupA=0.620
1000Genomes	American	Sub	694	- No frequency provided	dupA=0.684
Allele Frequency Aggregator	Total	Global	400	(A)₁₃=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	European	Sub	328	(A)₁₃=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	African	Sub	26	(A)₁₃=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Other	Sub	16	(A)₁₃=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Latin American 2	Sub	14	(A)₁₃=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Asian	Sub	8	(A)₁₃=1.0	delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0
Allele Frequency Aggregator	Latin American 1	Sub	4	(A)₁₃=1.0	delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0
Allele Frequency Aggregator	South Asian	Sub	4	(A)₁₃=1.0	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 12	NC_000012.12:g.113092338_113092339del
GRCh38.p14 chr 12	NC_000012.12:g.113092339del
GRCh38.p14 chr 12	NC_000012.12:g.113092339dup
GRCh38.p14 chr 12	NC_000012.12:g.113092338_113092339dup
GRCh38.p14 chr 12	NC_000012.12:g.113092337_113092339dup
GRCh37.p13 chr 12	NC_000012.11:g.113530143_113530144del
GRCh37.p13 chr 12	NC_000012.11:g.113530144del
GRCh37.p13 chr 12	NC_000012.11:g.113530144dup
GRCh37.p13 chr 12	NC_000012.11:g.113530143_113530144dup
GRCh37.p13 chr 12	NC_000012.11:g.113530142_113530144dup

Gene: DTX1, deltex E3 ubiquitin ligase 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
DTX1 transcript	NM_004416.3:c.942-824_942… NM_004416.3:c.942-824_942-823del	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)₁₃=	delAA	delA	dupA	dupAA	dupAAA
GRCh38.p14 chr 12	NC_000012.12:g.113092327_113092339=	NC_000012.12:g.113092338_113092339del	NC_000012.12:g.113092339del	NC_000012.12:g.113092339dup	NC_000012.12:g.113092338_113092339dup	NC_000012.12:g.113092337_113092339dup
GRCh37.p13 chr 12	NC_000012.11:g.113530132_113530144=	NC_000012.11:g.113530143_113530144del	NC_000012.11:g.113530144del	NC_000012.11:g.113530144dup	NC_000012.11:g.113530143_113530144dup	NC_000012.11:g.113530142_113530144dup
DTX1 transcript	NM_004416.2:c.942-835=	NM_004416.2:c.942-824_942-823del	NM_004416.2:c.942-823del	NM_004416.2:c.942-823dup	NM_004416.2:c.942-824_942-823dup	NM_004416.2:c.942-825_942-823dup
DTX1 transcript	NM_004416.3:c.942-835=	NM_004416.3:c.942-824_942-823del	NM_004416.3:c.942-823del	NM_004416.3:c.942-823dup	NM_004416.3:c.942-824_942-823dup	NM_004416.3:c.942-825_942-823dup
DTX1 transcript variant X1	XM_005253855.1:c.942-835=	XM_005253855.1:c.942-824_942-823del	XM_005253855.1:c.942-823del	XM_005253855.1:c.942-823dup	XM_005253855.1:c.942-824_942-823dup	XM_005253855.1:c.942-825_942-823dup

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#.

58 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40093206	Mar 14, 2006 (138)
2	HGSV	ss77841107	Oct 12, 2018 (152)
3	HGSV	ss79793082	Oct 12, 2018 (152)
4	HGSV	ss80335025	Oct 12, 2018 (152)
5	HGSV	ss82187609	Oct 12, 2018 (152)
6	HGSV	ss83451829	Oct 12, 2018 (152)
7	HGSV	ss83686195	Oct 12, 2018 (152)
8	HUMANGENOME_JCVI	ss95607687	Feb 06, 2009 (130)
9	HUMANGENOME_JCVI	ss97276268	Feb 06, 2009 (138)
10	GMI	ss287898047	May 09, 2011 (134)
11	GMI	ss289152893	May 04, 2012 (137)
12	PJP	ss294775053	May 09, 2011 (137)
13	BILGI_BIOE	ss666584166	Apr 25, 2013 (138)
14	1000GENOMES	ss1372628165	Aug 21, 2014 (142)
15	EVA_UK10K_ALSPAC	ss1707629681	Apr 01, 2015 (144)
16	EVA_UK10K_TWINSUK	ss1707629836	Apr 01, 2015 (144)
17	EVA_UK10K_TWINSUK	ss1710580506	Apr 01, 2015 (144)
18	EVA_UK10K_ALSPAC	ss1710580525	Apr 01, 2015 (144)
19	HAMMER_LAB	ss1807425221	Sep 08, 2015 (146)
20	SWEGEN	ss3010370597	Nov 08, 2017 (151)
21	EVA_DECODE	ss3694492959	Jul 13, 2019 (153)
22	EVA_DECODE	ss3694492960	Jul 13, 2019 (153)
23	EVA_DECODE	ss3694492961	Jul 13, 2019 (153)
24	EVA_DECODE	ss3694492962	Jul 13, 2019 (153)
25	ACPOP	ss3739392857	Jul 13, 2019 (153)
26	ACPOP	ss3739392858	Jul 13, 2019 (153)
27	PACBIO	ss3787339308	Jul 13, 2019 (153)
28	PACBIO	ss3787339309	Jul 13, 2019 (153)
29	PACBIO	ss3792420761	Jul 13, 2019 (153)
30	PACBIO	ss3792420762	Jul 13, 2019 (153)
31	PACBIO	ss3797303847	Jul 13, 2019 (153)
32	PACBIO	ss3797303848	Jul 13, 2019 (153)
33	KHV_HUMAN_GENOMES	ss3816311935	Jul 13, 2019 (153)
34	EVA	ss3833331790	Apr 27, 2020 (154)
35	EVA	ss3845726560	Apr 27, 2020 (154)
36	KOGIC	ss3972757818	Apr 27, 2020 (154)
37	KOGIC	ss3972757819	Apr 27, 2020 (154)
38	KOGIC	ss3972757820	Apr 27, 2020 (154)
39	GNOMAD	ss4259273681	Apr 26, 2021 (155)
40	GNOMAD	ss4259273682	Apr 26, 2021 (155)
41	GNOMAD	ss4259273683	Apr 26, 2021 (155)
42	GNOMAD	ss4259273685	Apr 26, 2021 (155)
43	GNOMAD	ss4259273686	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5208230018	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5208230019	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5208230020	Apr 26, 2021 (155)
47	1000G_HIGH_COVERAGE	ss5292280801	Oct 16, 2022 (156)
48	1000G_HIGH_COVERAGE	ss5292280802	Oct 16, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5292280803	Oct 16, 2022 (156)
50	HUGCELL_USP	ss5486879014	Oct 16, 2022 (156)
51	HUGCELL_USP	ss5486879015	Oct 16, 2022 (156)
52	TOMMO_GENOMICS	ss5758575297	Oct 16, 2022 (156)
53	TOMMO_GENOMICS	ss5758575298	Oct 16, 2022 (156)
54	TOMMO_GENOMICS	ss5758575299	Oct 16, 2022 (156)
55	EVA	ss5838532268	Oct 16, 2022 (156)
56	EVA	ss5838532269	Oct 16, 2022 (156)
57	EVA	ss5850552018	Oct 16, 2022 (156)
58	EVA	ss5906076515	Oct 16, 2022 (156)
59	1000Genomes	NC_000012.11 - 113530132	Oct 12, 2018 (152)
60	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 33049293 (NC_000012.11:113530131::A 2392/3854) Row 33049294 (NC_000012.11:113530131:A: 664/3854)	-	Oct 12, 2018 (152)
61	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 33049293 (NC_000012.11:113530131::A 2392/3854) Row 33049294 (NC_000012.11:113530131:A: 664/3854)	-	Oct 12, 2018 (152)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419758754 (NC_000012.12:113092326::A 93639/133928) Row 419758755 (NC_000012.12:113092326::AA 94/133988) Row 419758756 (NC_000012.12:113092326::AAA 1/134010)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419758754 (NC_000012.12:113092326::A 93639/133928) Row 419758755 (NC_000012.12:113092326::AA 94/133988) Row 419758756 (NC_000012.12:113092326::AAA 1/134010)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419758754 (NC_000012.12:113092326::A 93639/133928) Row 419758755 (NC_000012.12:113092326::AA 94/133988) Row 419758756 (NC_000012.12:113092326::AAA 1/134010)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419758754 (NC_000012.12:113092326::A 93639/133928) Row 419758755 (NC_000012.12:113092326::AA 94/133988) Row 419758756 (NC_000012.12:113092326::AAA 1/134010)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419758754 (NC_000012.12:113092326::A 93639/133928) Row 419758755 (NC_000012.12:113092326::AA 94/133988) Row 419758756 (NC_000012.12:113092326::AAA 1/134010)...	-	Apr 26, 2021 (155)
67	Korean Genome Project Submission ignored due to conflicting rows: Row 29135819 (NC_000012.12:113092327::A 1210/1832) Row 29135820 (NC_000012.12:113092327::AA 70/1832) Row 29135821 (NC_000012.12:113092326:A: 11/1832)	-	Apr 27, 2020 (154)
68	Korean Genome Project Submission ignored due to conflicting rows: Row 29135819 (NC_000012.12:113092327::A 1210/1832) Row 29135820 (NC_000012.12:113092327::AA 70/1832) Row 29135821 (NC_000012.12:113092326:A: 11/1832)	-	Apr 27, 2020 (154)
69	Korean Genome Project Submission ignored due to conflicting rows: Row 29135819 (NC_000012.12:113092327::A 1210/1832) Row 29135820 (NC_000012.12:113092327::AA 70/1832) Row 29135821 (NC_000012.12:113092326:A: 11/1832)	-	Apr 27, 2020 (154)
70	Northern Sweden Submission ignored due to conflicting rows: Row 12677722 (NC_000012.11:113530131::A 339/568) Row 12677723 (NC_000012.11:113530131:A: 81/568)	-	Jul 13, 2019 (153)
71	Northern Sweden Submission ignored due to conflicting rows: Row 12677722 (NC_000012.11:113530131::A 339/568) Row 12677723 (NC_000012.11:113530131:A: 81/568)	-	Jul 13, 2019 (153)
72	8.3KJPN Submission ignored due to conflicting rows: Row 66199325 (NC_000012.11:113530131::A 11965/16748) Row 66199326 (NC_000012.11:113530131:A: 14/16748) Row 66199327 (NC_000012.11:113530131::AA 16/16748)	-	Apr 26, 2021 (155)
73	8.3KJPN Submission ignored due to conflicting rows: Row 66199325 (NC_000012.11:113530131::A 11965/16748) Row 66199326 (NC_000012.11:113530131:A: 14/16748) Row 66199327 (NC_000012.11:113530131::AA 16/16748)	-	Apr 26, 2021 (155)
74	8.3KJPN Submission ignored due to conflicting rows: Row 66199325 (NC_000012.11:113530131::A 11965/16748) Row 66199326 (NC_000012.11:113530131:A: 14/16748) Row 66199327 (NC_000012.11:113530131::AA 16/16748)	-	Apr 26, 2021 (155)
75	14KJPN Submission ignored due to conflicting rows: Row 92412401 (NC_000012.12:113092326::A 20399/28258) Row 92412402 (NC_000012.12:113092326:A: 21/28258) Row 92412403 (NC_000012.12:113092326::AA 22/28258)	-	Oct 16, 2022 (156)
76	14KJPN Submission ignored due to conflicting rows: Row 92412401 (NC_000012.12:113092326::A 20399/28258) Row 92412402 (NC_000012.12:113092326:A: 21/28258) Row 92412403 (NC_000012.12:113092326::AA 22/28258)	-	Oct 16, 2022 (156)
77	14KJPN Submission ignored due to conflicting rows: Row 92412401 (NC_000012.12:113092326::A 20399/28258) Row 92412402 (NC_000012.12:113092326:A: 21/28258) Row 92412403 (NC_000012.12:113092326::AA 22/28258)	-	Oct 16, 2022 (156)
78	UK 10K study - Twins Submission ignored due to conflicting rows: Row 33049293 (NC_000012.11:113530131::A 2346/3708) Row 33049294 (NC_000012.11:113530131:A: 602/3708)	-	Oct 12, 2018 (152)
79	UK 10K study - Twins Submission ignored due to conflicting rows: Row 33049293 (NC_000012.11:113530131::A 2346/3708) Row 33049294 (NC_000012.11:113530131:A: 602/3708)	-	Oct 12, 2018 (152)
80	ALFA	NC_000012.12 - 113092327	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)
rs11397172	May 15, 2013 (138)
rs11397710	May 11, 2012 (137)
rs34327242	May 11, 2012 (137)
rs34395249	May 11, 2012 (137)
rs60577236	May 26, 2008 (130)
rs66741530	May 11, 2012 (137)
rs66741531	Feb 26, 2009 (130)
rs67079872	May 11, 2012 (137)
rs67079873	Feb 26, 2009 (130)
rs67079874	Feb 26, 2009 (130)
rs67079875	Feb 26, 2009 (130)
rs72294816	May 11, 2012 (137)
rs149220476	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3694492962, ss4259273686, ss5292280803	NC_000012.12:113092326:AA:	NC_000012.12:113092326:AAAAAAAAAAA… NC_000012.12:113092326:AAAAAAAAAAAAA:AAAAAAAAAAA	(self)
2426505477	NC_000012.12:113092326:AAAAAAAAAAA… NC_000012.12:113092326:AAAAAAAAAAAAA:AAAAAAAAAAA	NC_000012.12:113092326:AAAAAAAAAAA… NC_000012.12:113092326:AAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss1707629681, ss1707629836, ss3010370597, ss3739392858, ss3787339308, ss3792420761, ss3797303847, ss5208230019, ss5838532269	NC_000012.11:113530131:A:	NC_000012.12:113092326:AAAAAAAAAAA… NC_000012.12:113092326:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3972757820, ss4259273685, ss5292280802, ss5486879015, ss5758575298	NC_000012.12:113092326:A:	NC_000012.12:113092326:AAAAAAAAAAA… NC_000012.12:113092326:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
2426505477	NC_000012.12:113092326:AAAAAAAAAAA… NC_000012.12:113092326:AAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000012.12:113092326:AAAAAAAAAAA… NC_000012.12:113092326:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3694492961	NC_000012.12:113092327:A:	NC_000012.12:113092326:AAAAAAAAAAA… NC_000012.12:113092326:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss287898047	NT_009775.17:4106661:A:	NC_000012.12:113092326:AAAAAAAAAAA… NC_000012.12:113092326:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss294775053	NC_000012.10:112014521::A	NC_000012.12:113092326:AAAAAAAAAAA… NC_000012.12:113092326:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss289152893	NC_000012.10:112014527::A	NC_000012.12:113092326:AAAAAAAAAAA… NC_000012.12:113092326:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
59505066, ss666584166, ss1372628165, ss1807425221, ss3739392857, ss3787339309, ss3792420762, ss3797303848, ss3833331790, ss5208230018, ss5838532268	NC_000012.11:113530131::A	NC_000012.12:113092326:AAAAAAAAAAA… NC_000012.12:113092326:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss1710580506, ss1710580525	NC_000012.11:113530132::A	NC_000012.12:113092326:AAAAAAAAAAA… NC_000012.12:113092326:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3816311935, ss3845726560, ss4259273681, ss5292280801, ss5486879014, ss5758575297, ss5850552018, ss5906076515	NC_000012.12:113092326::A	NC_000012.12:113092326:AAAAAAAAAAA… NC_000012.12:113092326:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
2426505477	NC_000012.12:113092326:AAAAAAAAAAA… NC_000012.12:113092326:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000012.12:113092326:AAAAAAAAAAA… NC_000012.12:113092326:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3972757818	NC_000012.12:113092327::A	NC_000012.12:113092326:AAAAAAAAAAA… NC_000012.12:113092326:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3694492960	NC_000012.12:113092328::A	NC_000012.12:113092326:AAAAAAAAAAA… NC_000012.12:113092326:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss40093206, ss97276268	NT_009775.17:4106661::A	NC_000012.12:113092326:AAAAAAAAAAA… NC_000012.12:113092326:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss77841107, ss79793082, ss80335025, ss82187609, ss83451829, ss83686195, ss95607687	NT_009775.17:4106674::A	NC_000012.12:113092326:AAAAAAAAAAA… NC_000012.12:113092326:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss5208230020	NC_000012.11:113530131::AA	NC_000012.12:113092326:AAAAAAAAAAA… NC_000012.12:113092326:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4259273682, ss5758575299	NC_000012.12:113092326::AA	NC_000012.12:113092326:AAAAAAAAAAA… NC_000012.12:113092326:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
2426505477	NC_000012.12:113092326:AAAAAAAAAAA… NC_000012.12:113092326:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000012.12:113092326:AAAAAAAAAAA… NC_000012.12:113092326:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3972757819	NC_000012.12:113092327::AA	NC_000012.12:113092326:AAAAAAAAAAA… NC_000012.12:113092326:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3694492959	NC_000012.12:113092328::AA	NC_000012.12:113092326:AAAAAAAAAAA… NC_000012.12:113092326:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4259273683	NC_000012.12:113092326::AAA	NC_000012.12:113092326:AAAAAAAAAAA… NC_000012.12:113092326:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(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 rs11372823

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

rs11372823