Name: rs34137281
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.

rs34137281

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:115831925-115831941 (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)₄ / delAAA / delAA / delA / …
del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄
Variation Type: Indel Insertion and Deletion
Frequency: (A)₁₇=0.3034 (1602/5280, ALFA)
delAA=0.0662 (255/3854, ALSPAC)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NHLH2 : 3 Prime UTR 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	5280	AAAAAAAAAAAAAAAAA=0.3034	AAAAAAAAAAAAAAA=0.0040, AAAAAAAAAAAAAAAA=0.4405, AAAAAAAAAAAAAAAAAA=0.2521, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000	0.348955	0.394554	0.256491	32
European	Sub	4338	AAAAAAAAAAAAAAAAA=0.1540	AAAAAAAAAAAAAAA=0.0048, AAAAAAAAAAAAAAAA=0.5350, AAAAAAAAAAAAAAAAAA=0.3061, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000	0.075676	0.559459	0.364865	2
African	Sub	876	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	44	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	832	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	6	AAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	6	AAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	8	AAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	8	AAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
South Asian	Sub	2	AAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other	Sub	42	AAAAAAAAAAAAAAAAA=0.81	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.12, AAAAAAAAAAAAAAAAAA=0.07, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	0.894737	0.105263	0.0	11

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	5280	(A)₁₇=0.3034	delAA=0.0040, delA=0.4405, dupA=0.2521, dupAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	European	Sub	4338	(A)₁₇=0.1540	delAA=0.0048, delA=0.5350, dupA=0.3061, dupAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	African	Sub	876	(A)₁₇=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Other	Sub	42	(A)₁₇=0.81	delAA=0.00, delA=0.12, dupA=0.07, dupAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	Latin American 1	Sub	8	(A)₁₇=1.0	delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dup(A)₄=0.0
Allele Frequency Aggregator	Latin American 2	Sub	8	(A)₁₇=1.0	delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dup(A)₄=0.0
Allele Frequency Aggregator	Asian	Sub	6	(A)₁₇=1.0	delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dup(A)₄=0.0
Allele Frequency Aggregator	South Asian	Sub	2	(A)₁₇=1.0	delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dup(A)₄=0.0
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(A)₁₇=0.9338	delAA=0.0662

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.115831938_115831941del
GRCh38.p14 chr 1	NC_000001.11:g.115831939_115831941del
GRCh38.p14 chr 1	NC_000001.11:g.115831940_115831941del
GRCh38.p14 chr 1	NC_000001.11:g.115831941del
GRCh38.p14 chr 1	NC_000001.11:g.115831941dup
GRCh38.p14 chr 1	NC_000001.11:g.115831940_115831941dup
GRCh38.p14 chr 1	NC_000001.11:g.115831939_115831941dup
GRCh38.p14 chr 1	NC_000001.11:g.115831938_115831941dup
GRCh37.p13 chr 1	NC_000001.10:g.116374559_116374562del
GRCh37.p13 chr 1	NC_000001.10:g.116374560_116374562del
GRCh37.p13 chr 1	NC_000001.10:g.116374561_116374562del
GRCh37.p13 chr 1	NC_000001.10:g.116374562del
GRCh37.p13 chr 1	NC_000001.10:g.116374562dup
GRCh37.p13 chr 1	NC_000001.10:g.116374561_116374562dup
GRCh37.p13 chr 1	NC_000001.10:g.116374560_116374562dup
GRCh37.p13 chr 1	NC_000001.10:g.116374559_116374562dup

Gene: NHLH2, nescient helix-loop-helix 2 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NHLH2 transcript variant 2	NM_001111061.2:c.	N/A	Genic Downstream Transcript Variant
NHLH2 transcript variant 1	NM_005599.3:c.	N/A	Genic Downstream Transcript Variant
NHLH2 transcript variant X1	XM_047421407.1:c.2781_2… XM_047421407.1:c.2781_2797=	N/A	3 Prime UTR 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)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄
GRCh38.p14 chr 1	NC_000001.11:g.115831925_115831941=	NC_000001.11:g.115831938_115831941del	NC_000001.11:g.115831939_115831941del	NC_000001.11:g.115831940_115831941del	NC_000001.11:g.115831941del	NC_000001.11:g.115831941dup	NC_000001.11:g.115831940_115831941dup	NC_000001.11:g.115831939_115831941dup	NC_000001.11:g.115831938_115831941dup
GRCh37.p13 chr 1	NC_000001.10:g.116374546_116374562=	NC_000001.10:g.116374559_116374562del	NC_000001.10:g.116374560_116374562del	NC_000001.10:g.116374561_116374562del	NC_000001.10:g.116374562del	NC_000001.10:g.116374562dup	NC_000001.10:g.116374561_116374562dup	NC_000001.10:g.116374560_116374562dup	NC_000001.10:g.116374559_116374562dup
NHLH2 transcript variant X1	XM_047421407.1:c.2781_2797=	XM_047421407.1:c.2794_2797del	XM_047421407.1:c.2795_2797del	XM_047421407.1:c.2796_2797del	XM_047421407.1:c.*2797del	XM_047421407.1:c.*2797dup	XM_047421407.1:c.2796_2797dup	XM_047421407.1:c.2795_2797dup	XM_047421407.1:c.2794_2797dup

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#.

52 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41073398	Mar 13, 2006 (126)
2	ABI	ss41288685	Mar 15, 2006 (144)
3	HGSV	ss82184291	Dec 14, 2007 (137)
4	HUMANGENOME_JCVI	ss95241333	Feb 13, 2009 (144)
5	GMI	ss288030169	May 04, 2012 (137)
6	GMI	ss288030171	Jan 10, 2018 (151)
7	PJP	ss294599978	Jan 10, 2018 (151)
8	PJP	ss294599979	Jan 10, 2018 (151)
9	EVA_UK10K_ALSPAC	ss1701150345	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1701150377	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1709946345	Apr 01, 2015 (144)
12	EVA_UK10K_ALSPAC	ss1709946366	Apr 01, 2015 (144)
13	SYSTEMSBIOZJU	ss2624472514	Nov 08, 2017 (151)
14	SWEGEN	ss2987489821	Nov 08, 2017 (151)
15	BIOINF_KMB_FNS_UNIBA	ss3645067721	Oct 11, 2018 (152)
16	URBANLAB	ss3646759463	Oct 11, 2018 (152)
17	EVA_DECODE	ss3687592627	Jul 12, 2019 (153)
18	EVA_DECODE	ss3687592628	Jul 12, 2019 (153)
19	EVA_DECODE	ss3687592629	Jul 12, 2019 (153)
20	EVA_DECODE	ss3687592630	Jul 12, 2019 (153)
21	EVA_DECODE	ss3687592631	Jul 12, 2019 (153)
22	ACPOP	ss3727416214	Jul 12, 2019 (153)
23	ACPOP	ss3727416215	Jul 12, 2019 (153)
24	ACPOP	ss3727416216	Jul 12, 2019 (153)
25	PACBIO	ss3783528362	Jul 12, 2019 (153)
26	PACBIO	ss3789168753	Jul 12, 2019 (153)
27	PACBIO	ss3794041704	Jul 12, 2019 (153)
28	EVA	ss3826386431	Apr 25, 2020 (154)
29	GNOMAD	ss4000988913	Apr 25, 2021 (155)
30	GNOMAD	ss4000988914	Apr 25, 2021 (155)
31	GNOMAD	ss4000988915	Apr 25, 2021 (155)
32	GNOMAD	ss4000988916	Apr 25, 2021 (155)
33	GNOMAD	ss4000988918	Apr 25, 2021 (155)
34	GNOMAD	ss4000988919	Apr 25, 2021 (155)
35	GNOMAD	ss4000988920	Apr 25, 2021 (155)
36	GNOMAD	ss4000988921	Apr 25, 2021 (155)
37	TOMMO_GENOMICS	ss5145821561	Apr 25, 2021 (155)
38	TOMMO_GENOMICS	ss5145821562	Apr 25, 2021 (155)
39	TOMMO_GENOMICS	ss5145821563	Apr 25, 2021 (155)
40	1000G_HIGH_COVERAGE	ss5243717033	Oct 12, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5243717034	Oct 12, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5243717035	Oct 12, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5243717036	Oct 12, 2022 (156)
44	HUGCELL_USP	ss5444630635	Oct 12, 2022 (156)
45	HUGCELL_USP	ss5444630636	Oct 12, 2022 (156)
46	HUGCELL_USP	ss5444630637	Oct 12, 2022 (156)
47	TOMMO_GENOMICS	ss5671132179	Oct 12, 2022 (156)
48	TOMMO_GENOMICS	ss5671132180	Oct 12, 2022 (156)
49	TOMMO_GENOMICS	ss5671132181	Oct 12, 2022 (156)
50	TOMMO_GENOMICS	ss5671132182	Oct 12, 2022 (156)
51	EVA	ss5832526234	Oct 12, 2022 (156)
52	EVA	ss5909926323	Oct 12, 2022 (156)
53	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 116374546	Oct 11, 2018 (152)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 23608709 (NC_000001.11:115831924::A 32420/125908) Row 23608710 (NC_000001.11:115831924::AA 342/126130) Row 23608711 (NC_000001.11:115831924::AAA 1/126142)...	-	Apr 25, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 23608709 (NC_000001.11:115831924::A 32420/125908) Row 23608710 (NC_000001.11:115831924::AA 342/126130) Row 23608711 (NC_000001.11:115831924::AAA 1/126142)...	-	Apr 25, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 23608709 (NC_000001.11:115831924::A 32420/125908) Row 23608710 (NC_000001.11:115831924::AA 342/126130) Row 23608711 (NC_000001.11:115831924::AAA 1/126142)...	-	Apr 25, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 23608709 (NC_000001.11:115831924::A 32420/125908) Row 23608710 (NC_000001.11:115831924::AA 342/126130) Row 23608711 (NC_000001.11:115831924::AAA 1/126142)...	-	Apr 25, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 23608709 (NC_000001.11:115831924::A 32420/125908) Row 23608710 (NC_000001.11:115831924::AA 342/126130) Row 23608711 (NC_000001.11:115831924::AAA 1/126142)...	-	Apr 25, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 23608709 (NC_000001.11:115831924::A 32420/125908) Row 23608710 (NC_000001.11:115831924::AA 342/126130) Row 23608711 (NC_000001.11:115831924::AAA 1/126142)...	-	Apr 25, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 23608709 (NC_000001.11:115831924::A 32420/125908) Row 23608710 (NC_000001.11:115831924::AA 342/126130) Row 23608711 (NC_000001.11:115831924::AAA 1/126142)...	-	Apr 25, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 23608709 (NC_000001.11:115831924::A 32420/125908) Row 23608710 (NC_000001.11:115831924::AA 342/126130) Row 23608711 (NC_000001.11:115831924::AAA 1/126142)...	-	Apr 25, 2021 (155)
62	Northern Sweden Submission ignored due to conflicting rows: Row 701079 (NC_000001.10:116374545:A: 343/580) Row 701080 (NC_000001.10:116374545::A 155/580) Row 701081 (NC_000001.10:116374545:AA: 8/580)	-	Jul 12, 2019 (153)
63	Northern Sweden Submission ignored due to conflicting rows: Row 701079 (NC_000001.10:116374545:A: 343/580) Row 701080 (NC_000001.10:116374545::A 155/580) Row 701081 (NC_000001.10:116374545:AA: 8/580)	-	Jul 12, 2019 (153)
64	Northern Sweden Submission ignored due to conflicting rows: Row 701079 (NC_000001.10:116374545:A: 343/580) Row 701080 (NC_000001.10:116374545::A 155/580) Row 701081 (NC_000001.10:116374545:AA: 8/580)	-	Jul 12, 2019 (153)
65	8.3KJPN Submission ignored due to conflicting rows: Row 3790868 (NC_000001.10:116374545::A 7117/16758) Row 3790869 (NC_000001.10:116374545:A: 6155/16758) Row 3790870 (NC_000001.10:116374545::AA 27/16758)	-	Apr 25, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 3790868 (NC_000001.10:116374545::A 7117/16758) Row 3790869 (NC_000001.10:116374545:A: 6155/16758) Row 3790870 (NC_000001.10:116374545::AA 27/16758)	-	Apr 25, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 3790868 (NC_000001.10:116374545::A 7117/16758) Row 3790869 (NC_000001.10:116374545:A: 6155/16758) Row 3790870 (NC_000001.10:116374545::AA 27/16758)	-	Apr 25, 2021 (155)
68	14KJPN Submission ignored due to conflicting rows: Row 4969283 (NC_000001.11:115831924:A: 10347/28256) Row 4969284 (NC_000001.11:115831924::A 12022/28256) Row 4969285 (NC_000001.11:115831924:AA: 9/28256)...	-	Oct 12, 2022 (156)
69	14KJPN Submission ignored due to conflicting rows: Row 4969283 (NC_000001.11:115831924:A: 10347/28256) Row 4969284 (NC_000001.11:115831924::A 12022/28256) Row 4969285 (NC_000001.11:115831924:AA: 9/28256)...	-	Oct 12, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 4969283 (NC_000001.11:115831924:A: 10347/28256) Row 4969284 (NC_000001.11:115831924::A 12022/28256) Row 4969285 (NC_000001.11:115831924:AA: 9/28256)...	-	Oct 12, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 4969283 (NC_000001.11:115831924:A: 10347/28256) Row 4969284 (NC_000001.11:115831924::A 12022/28256) Row 4969285 (NC_000001.11:115831924:AA: 9/28256)...	-	Oct 12, 2022 (156)
72	UK 10K study - Twins Submission ignored due to conflicting rows: Row 1848616 (NC_000001.10:116374546:A: 3255/3708) Row 1848617 (NC_000001.10:116374545:AA: 255/3708)	-	Apr 25, 2020 (154)
73	UK 10K study - Twins	-	Oct 11, 2018 (152)
74	ALFA	NC_000001.11 - 115831925	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)
rs35491703	Jul 01, 2015 (144)
rs57785731	May 11, 2012 (137)
rs67347572	May 15, 2013 (138)
rs67347573	Feb 27, 2009 (130)
rs67419551	May 11, 2012 (137)
rs67419552	Feb 27, 2009 (130)
rs67419553	Feb 27, 2009 (130)
rs71096839	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4000988921	NC_000001.11:115831924:AAAA:	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3687592631, ss4000988920	NC_000001.11:115831924:AAA:	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
1848617, ss1701150345, ss1701150377, ss2987489821, ss3727416216	NC_000001.10:116374545:AA:	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4000988919, ss5243717036, ss5444630637, ss5671132181	NC_000001.11:115831924:AA:	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
6405138148	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3687592630	NC_000001.11:115831925:AA:	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss82184291	NC_000001.8:116086603:A:	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss288030169	NC_000001.9:116176068:A:	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss2624472514, ss3727416214, ss3783528362, ss3789168753, ss3794041704, ss3826386431, ss5145821562, ss5832526234	NC_000001.10:116374545:A:	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss1709946345, ss1709946366	NC_000001.10:116374546:A:	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3645067721, ss4000988918, ss5243717034, ss5444630635, ss5671132179, ss5909926323	NC_000001.11:115831924:A:	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
6405138148	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3687592629	NC_000001.11:115831926:A:	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss41073398	NT_032977.9:86346463:A:	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss294599978	NC_000001.9:116176069::A	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss288030171, ss294599979	NC_000001.9:116176085::A	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3727416215, ss5145821561	NC_000001.10:116374545::A	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3646759463, ss4000988913, ss5243717033, ss5444630636, ss5671132180	NC_000001.11:115831924::A	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
6405138148	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3687592628	NC_000001.11:115831927::A	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss41288685	NT_032977.9:86346463::A	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss95241333	NT_032977.9:86346480::A	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss5145821563	NC_000001.10:116374545::AA	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4000988914, ss5243717035, ss5671132182	NC_000001.11:115831924::AA	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
6405138148	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3687592627	NC_000001.11:115831927::AA	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4000988915	NC_000001.11:115831924::AAA	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4000988916	NC_000001.11:115831924::AAAA	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
6405138148	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000001.11:115831924:AAAAAAAAAAA… NC_000001.11:115831924:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(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 rs34137281

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

rs34137281