Name: rs34462401
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.

rs34462401

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr12:45049663-45049677 (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 / dupAAA
Variation Type: Indel Insertion and Deletion
Frequency: delAAA=0.0000 (0/3278, ALFA)
delAA=0.0000 (0/3278, ALFA)
delA=0.0000 (0/3278, ALFA) (+ 4 more)
dupA=0.0000 (0/3278, ALFA)
dupAA=0.0000 (0/3278, ALFA)
dupAAA=0.0000 (0/3278, ALFA)
dupA=0.447 (251/562, NorthernSweden)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: DBX2 : 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	3278	AAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	2072	AAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	768	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	14	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	754	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	12	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	8	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Other Asian	Sub	4	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	46	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	274	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	4	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Other	Sub	102	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, 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	3278	(A)₁₅=1.0000	delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	European	Sub	2072	(A)₁₅=1.0000	delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	African	Sub	768	(A)₁₅=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Latin American 2	Sub	274	(A)₁₅=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Other	Sub	102	(A)₁₅=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	46	(A)₁₅=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Asian	Sub	12	(A)₁₅=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	South Asian	Sub	4	(A)₁₅=1.0	delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0
Northern Sweden	ACPOP	Study-wide	562	- No frequency provided	dupA=0.447

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.45049675_45049677del
GRCh38.p14 chr 12	NC_000012.12:g.45049676_45049677del
GRCh38.p14 chr 12	NC_000012.12:g.45049677del
GRCh38.p14 chr 12	NC_000012.12:g.45049677dup
GRCh38.p14 chr 12	NC_000012.12:g.45049676_45049677dup
GRCh38.p14 chr 12	NC_000012.12:g.45049675_45049677dup
GRCh37.p13 chr 12	NC_000012.11:g.45443458_45443460del
GRCh37.p13 chr 12	NC_000012.11:g.45443459_45443460del
GRCh37.p13 chr 12	NC_000012.11:g.45443460del
GRCh37.p13 chr 12	NC_000012.11:g.45443460dup
GRCh37.p13 chr 12	NC_000012.11:g.45443459_45443460dup
GRCh37.p13 chr 12	NC_000012.11:g.45443458_45443460dup

Gene: DBX2, developing brain homeobox 2 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
DBX2 transcript	NM_001004329.3:c.403+860_… NM_001004329.3:c.403+860_403+862del	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)₁₅=	delAAA	delAA	delA	dupA	dupAA	dupAAA
GRCh38.p14 chr 12	NC_000012.12:g.45049663_45049677=	NC_000012.12:g.45049675_45049677del	NC_000012.12:g.45049676_45049677del	NC_000012.12:g.45049677del	NC_000012.12:g.45049677dup	NC_000012.12:g.45049676_45049677dup	NC_000012.12:g.45049675_45049677dup
GRCh37.p13 chr 12	NC_000012.11:g.45443446_45443460=	NC_000012.11:g.45443458_45443460del	NC_000012.11:g.45443459_45443460del	NC_000012.11:g.45443460del	NC_000012.11:g.45443460dup	NC_000012.11:g.45443459_45443460dup	NC_000012.11:g.45443458_45443460dup
DBX2 transcript	NM_001004329.2:c.403+862=	NM_001004329.2:c.403+860_403+862del	NM_001004329.2:c.403+861_403+862del	NM_001004329.2:c.403+862del	NM_001004329.2:c.403+862dup	NM_001004329.2:c.403+861_403+862dup	NM_001004329.2:c.403+860_403+862dup
DBX2 transcript	NM_001004329.3:c.403+862=	NM_001004329.3:c.403+860_403+862del	NM_001004329.3:c.403+861_403+862del	NM_001004329.3:c.403+862del	NM_001004329.3:c.403+862dup	NM_001004329.3:c.403+861_403+862dup	NM_001004329.3:c.403+860_403+862dup

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#.

49 SubSNP, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40166471	Mar 13, 2006 (126)
2	BUSHMAN	ss193275644	Jul 04, 2010 (144)
3	GMI	ss289125904	May 04, 2012 (144)
4	GMI	ss289125905	Jan 10, 2018 (151)
5	PJP	ss294749387	Jan 10, 2018 (151)
6	PJP	ss294749388	Jan 10, 2018 (151)
7	SSMP	ss664122517	Apr 01, 2015 (144)
8	JJLAB	ss2031130560	Sep 14, 2016 (149)
9	SYSTEMSBIOZJU	ss2628068528	Nov 08, 2017 (151)
10	SWEGEN	ss3009613260	Nov 08, 2017 (151)
11	SWEGEN	ss3009613261	Nov 08, 2017 (151)
12	MCHAISSO	ss3065474054	Nov 08, 2017 (151)
13	URBANLAB	ss3649828990	Oct 12, 2018 (152)
14	EVA_DECODE	ss3693581964	Jul 13, 2019 (153)
15	EVA_DECODE	ss3693581965	Jul 13, 2019 (153)
16	EVA_DECODE	ss3693581966	Jul 13, 2019 (153)
17	ACPOP	ss3738983250	Jul 13, 2019 (153)
18	EVA	ss3833100682	Apr 27, 2020 (154)
19	EVA	ss3840121191	Apr 27, 2020 (154)
20	EVA	ss3845607303	Apr 27, 2020 (154)
21	KOGIC	ss3971835326	Apr 27, 2020 (154)
22	KOGIC	ss3971835327	Apr 27, 2020 (154)
23	KOGIC	ss3971835328	Apr 27, 2020 (154)
24	GNOMAD	ss4250998083	Apr 26, 2021 (155)
25	GNOMAD	ss4250998084	Apr 26, 2021 (155)
26	GNOMAD	ss4250998085	Apr 26, 2021 (155)
27	GNOMAD	ss4250998086	Apr 26, 2021 (155)
28	GNOMAD	ss4250998087	Apr 26, 2021 (155)
29	GNOMAD	ss4250998088	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5206108614	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5206108615	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5206108616	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5206108617	Apr 26, 2021 (155)
34	1000G_HIGH_COVERAGE	ss5290648825	Oct 16, 2022 (156)
35	1000G_HIGH_COVERAGE	ss5290648826	Oct 16, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5290648827	Oct 16, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5290648828	Oct 16, 2022 (156)
38	1000G_HIGH_COVERAGE	ss5290648829	Oct 16, 2022 (156)
39	HUGCELL_USP	ss5485421355	Oct 16, 2022 (156)
40	HUGCELL_USP	ss5485421356	Oct 16, 2022 (156)
41	HUGCELL_USP	ss5485421357	Oct 16, 2022 (156)
42	HUGCELL_USP	ss5485421358	Oct 16, 2022 (156)
43	HUGCELL_USP	ss5485421359	Oct 16, 2022 (156)
44	TOMMO_GENOMICS	ss5755833881	Oct 16, 2022 (156)
45	TOMMO_GENOMICS	ss5755833882	Oct 16, 2022 (156)
46	TOMMO_GENOMICS	ss5755833883	Oct 16, 2022 (156)
47	TOMMO_GENOMICS	ss5755833884	Oct 16, 2022 (156)
48	EVA	ss5837907266	Oct 16, 2022 (156)
49	EVA	ss5904211664	Oct 16, 2022 (156)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 405999379 (NC_000012.12:45049662::A 55598/128078) Row 405999380 (NC_000012.12:45049662::AA 1765/128156) Row 405999381 (NC_000012.12:45049662::AAA 316/128206)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 405999379 (NC_000012.12:45049662::A 55598/128078) Row 405999380 (NC_000012.12:45049662::AA 1765/128156) Row 405999381 (NC_000012.12:45049662::AAA 316/128206)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 405999379 (NC_000012.12:45049662::A 55598/128078) Row 405999380 (NC_000012.12:45049662::AA 1765/128156) Row 405999381 (NC_000012.12:45049662::AAA 316/128206)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 405999379 (NC_000012.12:45049662::A 55598/128078) Row 405999380 (NC_000012.12:45049662::AA 1765/128156) Row 405999381 (NC_000012.12:45049662::AAA 316/128206)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 405999379 (NC_000012.12:45049662::A 55598/128078) Row 405999380 (NC_000012.12:45049662::AA 1765/128156) Row 405999381 (NC_000012.12:45049662::AAA 316/128206)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 405999379 (NC_000012.12:45049662::A 55598/128078) Row 405999380 (NC_000012.12:45049662::AA 1765/128156) Row 405999381 (NC_000012.12:45049662::AAA 316/128206)...	-	Apr 26, 2021 (155)
56	Korean Genome Project Submission ignored due to conflicting rows: Row 28213327 (NC_000012.12:45049663::A 638/1832) Row 28213328 (NC_000012.12:45049662:A: 284/1832) Row 28213329 (NC_000012.12:45049663::AA 33/1832)	-	Apr 27, 2020 (154)
57	Korean Genome Project Submission ignored due to conflicting rows: Row 28213327 (NC_000012.12:45049663::A 638/1832) Row 28213328 (NC_000012.12:45049662:A: 284/1832) Row 28213329 (NC_000012.12:45049663::AA 33/1832)	-	Apr 27, 2020 (154)
58	Korean Genome Project Submission ignored due to conflicting rows: Row 28213327 (NC_000012.12:45049663::A 638/1832) Row 28213328 (NC_000012.12:45049662:A: 284/1832) Row 28213329 (NC_000012.12:45049663::AA 33/1832)	-	Apr 27, 2020 (154)
59	Northern Sweden	NC_000012.11 - 45443446	Jul 13, 2019 (153)
60	8.3KJPN Submission ignored due to conflicting rows: Row 64077921 (NC_000012.11:45443445:A: 3324/16760) Row 64077922 (NC_000012.11:45443445::A 5951/16760) Row 64077923 (NC_000012.11:45443445::AA 150/16760)...	-	Apr 26, 2021 (155)
61	8.3KJPN Submission ignored due to conflicting rows: Row 64077921 (NC_000012.11:45443445:A: 3324/16760) Row 64077922 (NC_000012.11:45443445::A 5951/16760) Row 64077923 (NC_000012.11:45443445::AA 150/16760)...	-	Apr 26, 2021 (155)
62	8.3KJPN Submission ignored due to conflicting rows: Row 64077921 (NC_000012.11:45443445:A: 3324/16760) Row 64077922 (NC_000012.11:45443445::A 5951/16760) Row 64077923 (NC_000012.11:45443445::AA 150/16760)...	-	Apr 26, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 64077921 (NC_000012.11:45443445:A: 3324/16760) Row 64077922 (NC_000012.11:45443445::A 5951/16760) Row 64077923 (NC_000012.11:45443445::AA 150/16760)...	-	Apr 26, 2021 (155)
64	14KJPN Submission ignored due to conflicting rows: Row 89670985 (NC_000012.12:45049662::A 10009/28258) Row 89670986 (NC_000012.12:45049662:A: 5680/28258) Row 89670987 (NC_000012.12:45049662::AA 248/28258)...	-	Oct 16, 2022 (156)
65	14KJPN Submission ignored due to conflicting rows: Row 89670985 (NC_000012.12:45049662::A 10009/28258) Row 89670986 (NC_000012.12:45049662:A: 5680/28258) Row 89670987 (NC_000012.12:45049662::AA 248/28258)...	-	Oct 16, 2022 (156)
66	14KJPN Submission ignored due to conflicting rows: Row 89670985 (NC_000012.12:45049662::A 10009/28258) Row 89670986 (NC_000012.12:45049662:A: 5680/28258) Row 89670987 (NC_000012.12:45049662::AA 248/28258)...	-	Oct 16, 2022 (156)
67	14KJPN Submission ignored due to conflicting rows: Row 89670985 (NC_000012.12:45049662::A 10009/28258) Row 89670986 (NC_000012.12:45049662:A: 5680/28258) Row 89670987 (NC_000012.12:45049662::AA 248/28258)...	-	Oct 16, 2022 (156)
68	ALFA	NC_000012.12 - 45049663	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)
rs111765669	Jul 01, 2015 (144)
rs139609799	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4250998088	NC_000012.12:45049662:AAA:	NC_000012.12:45049662:AAAAAAAAAAAA… NC_000012.12:45049662:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
4220116337	NC_000012.12:45049662:AAAAAAAAAAAA… NC_000012.12:45049662:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000012.12:45049662:AAAAAAAAAAAA… NC_000012.12:45049662:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4250998087, ss5290648829, ss5485421358	NC_000012.12:45049662:AA:	NC_000012.12:45049662:AAAAAAAAAAAA… NC_000012.12:45049662:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
4220116337	NC_000012.12:45049662:AAAAAAAAAAAA… NC_000012.12:45049662:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000012.12:45049662:AAAAAAAAAAAA… NC_000012.12:45049662:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss289125904	NC_000012.10:43729712:A:	NC_000012.12:45049662:AAAAAAAAAAAA… NC_000012.12:45049662:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3833100682, ss5206108614	NC_000012.11:45443445:A:	NC_000012.12:45049662:AAAAAAAAAAAA… NC_000012.12:45049662:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3065474054, ss3693581966, ss3971835327, ss4250998086, ss5290648826, ss5485421355, ss5755833882	NC_000012.12:45049662:A:	NC_000012.12:45049662:AAAAAAAAAAAA… NC_000012.12:45049662:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
4220116337	NC_000012.12:45049662:AAAAAAAAAAAA… NC_000012.12:45049662:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000012.12:45049662:AAAAAAAAAAAA… NC_000012.12:45049662:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss193275644	NT_029419.13:7814410:A:	NC_000012.12:45049662:AAAAAAAAAAAA… NC_000012.12:45049662:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss294749387	NC_000012.10:43729713::A	NC_000012.12:45049662:AAAAAAAAAAAA… NC_000012.12:45049662:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss289125905, ss294749388	NC_000012.10:43729727::A	NC_000012.12:45049662:AAAAAAAAAAAA… NC_000012.12:45049662:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
12268115, ss664122517, ss2031130560, ss2628068528, ss3009613260, ss3738983250, ss3840121191, ss5206108615, ss5837907266	NC_000012.11:45443445::A	NC_000012.12:45049662:AAAAAAAAAAAA… NC_000012.12:45049662:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3649828990, ss3845607303, ss4250998083, ss5290648825, ss5485421356, ss5755833881, ss5904211664	NC_000012.12:45049662::A	NC_000012.12:45049662:AAAAAAAAAAAA… NC_000012.12:45049662:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
4220116337	NC_000012.12:45049662:AAAAAAAAAAAA… NC_000012.12:45049662:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000012.12:45049662:AAAAAAAAAAAA… NC_000012.12:45049662:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3693581965, ss3971835326	NC_000012.12:45049663::A	NC_000012.12:45049662:AAAAAAAAAAAA… NC_000012.12:45049662:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss40166471	NT_029419.12:7586751::A	NC_000012.12:45049662:AAAAAAAAAAAA… NC_000012.12:45049662:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3009613261, ss5206108616	NC_000012.11:45443445::AA	NC_000012.12:45049662:AAAAAAAAAAAA… NC_000012.12:45049662:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4250998084, ss5290648828, ss5485421357, ss5755833883	NC_000012.12:45049662::AA	NC_000012.12:45049662:AAAAAAAAAAAA… NC_000012.12:45049662:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
4220116337	NC_000012.12:45049662:AAAAAAAAAAAA… NC_000012.12:45049662:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000012.12:45049662:AAAAAAAAAAAA… NC_000012.12:45049662:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3693581964, ss3971835328	NC_000012.12:45049663::AA	NC_000012.12:45049662:AAAAAAAAAAAA… NC_000012.12:45049662:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss5206108617	NC_000012.11:45443445::AAA	NC_000012.12:45049662:AAAAAAAAAAAA… NC_000012.12:45049662:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4250998085, ss5290648827, ss5485421359, ss5755833884	NC_000012.12:45049662::AAA	NC_000012.12:45049662:AAAAAAAAAAAA… NC_000012.12:45049662:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
4220116337	NC_000012.12:45049662:AAAAAAAAAAAA… NC_000012.12:45049662:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000012.12:45049662:AAAAAAAAAAAA… NC_000012.12:45049662:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(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 rs34462401

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

rs34462401