Name: rs34279043
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.

rs34279043

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:73766310-73766323 (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 / dup(A)₄ / dup(A)₈
Variation Type: Indel Insertion and Deletion
Frequency: delAAA=0.0022 (5/2255, 1000G)
delAA=0.0000 (0/2100, ALFA)
delA=0.0000 (0/2100, ALFA) (+ 4 more)
dupA=0.0000 (0/2100, ALFA)
dupAA=0.0000 (0/2100, ALFA)
(A)₁₄=0.363 (209/576, NorthernSweden)
(A)₁₄=0.47 (19/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: DUSP11 : 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	2100	AAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	912	AAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000	1.0	N/A
African	Sub	946	AAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	48	AAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	898	AAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	16	AAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	10	AAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0	1.0	N/A
Other Asian	Sub	6	AAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	18	AAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	112	AAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	14	AAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	82	AAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00	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
1000Genomes	Global	Study-wide	2255	(A)₁₄=0.9978	delAAA=0.0022
1000Genomes	African	Sub	711	(A)₁₄=1.000	delAAA=0.000
1000Genomes	East Asian	Sub	427	(A)₁₄=0.998	delAAA=0.002
1000Genomes	Europe	Sub	405	(A)₁₄=0.998	delAAA=0.002
1000Genomes	South Asian	Sub	404	(A)₁₄=0.993	delAAA=0.007
1000Genomes	American	Sub	308	(A)₁₄=1.000	delAAA=0.000
Allele Frequency Aggregator	Total	Global	2100	(A)₁₄=1.0000	delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	African	Sub	946	(A)₁₄=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	European	Sub	912	(A)₁₄=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Latin American 2	Sub	112	(A)₁₄=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Other	Sub	82	(A)₁₄=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	18	(A)₁₄=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Asian	Sub	16	(A)₁₄=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	South Asian	Sub	14	(A)₁₄=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Northern Sweden	ACPOP	Study-wide	576	(A)₁₄=0.363	delA=0.637
The Danish reference pan genome	Danish	Study-wide	40	(A)₁₄=0.47	delA=0.53

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.73766321_73766323del
GRCh38.p14 chr 2	NC_000002.12:g.73766322_73766323del
GRCh38.p14 chr 2	NC_000002.12:g.73766323del
GRCh38.p14 chr 2	NC_000002.12:g.73766323dup
GRCh38.p14 chr 2	NC_000002.12:g.73766322_73766323dup
GRCh38.p14 chr 2	NC_000002.12:g.73766321_73766323dup
GRCh38.p14 chr 2	NC_000002.12:g.73766320_73766323dup
GRCh38.p14 chr 2	NC_000002.12:g.73766316_73766323dup
GRCh37.p13 chr 2	NC_000002.11:g.73993448_73993450del
GRCh37.p13 chr 2	NC_000002.11:g.73993449_73993450del
GRCh37.p13 chr 2	NC_000002.11:g.73993450del
GRCh37.p13 chr 2	NC_000002.11:g.73993450dup
GRCh37.p13 chr 2	NC_000002.11:g.73993449_73993450dup
GRCh37.p13 chr 2	NC_000002.11:g.73993448_73993450dup
GRCh37.p13 chr 2	NC_000002.11:g.73993447_73993450dup
GRCh37.p13 chr 2	NC_000002.11:g.73993443_73993450dup
GRCh38.p14 chr 2 fix patch HG2052_PATCH	NW_025791766.1:g.435819_435821del
GRCh38.p14 chr 2 fix patch HG2052_PATCH	NW_025791766.1:g.435820_435821del
GRCh38.p14 chr 2 fix patch HG2052_PATCH	NW_025791766.1:g.435821del
GRCh38.p14 chr 2 fix patch HG2052_PATCH	NW_025791766.1:g.435821dup
GRCh38.p14 chr 2 fix patch HG2052_PATCH	NW_025791766.1:g.435820_435821dup
GRCh38.p14 chr 2 fix patch HG2052_PATCH	NW_025791766.1:g.435819_435821dup
GRCh38.p14 chr 2 fix patch HG2052_PATCH	NW_025791766.1:g.435818_435821dup
GRCh38.p14 chr 2 fix patch HG2052_PATCH	NW_025791766.1:g.435814_435821dup

Gene: DUSP11, dual specificity phosphatase 11 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
DUSP11 transcript variant 1	NM_003584.3:c.794+106_794… NM_003584.3:c.794+106_794+108del	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)₁₄=	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₈
GRCh38.p14 chr 2	NC_000002.12:g.73766310_73766323=	NC_000002.12:g.73766321_73766323del	NC_000002.12:g.73766322_73766323del	NC_000002.12:g.73766323del	NC_000002.12:g.73766323dup	NC_000002.12:g.73766322_73766323dup	NC_000002.12:g.73766321_73766323dup	NC_000002.12:g.73766320_73766323dup	NC_000002.12:g.73766316_73766323dup
GRCh37.p13 chr 2	NC_000002.11:g.73993437_73993450=	NC_000002.11:g.73993448_73993450del	NC_000002.11:g.73993449_73993450del	NC_000002.11:g.73993450del	NC_000002.11:g.73993450dup	NC_000002.11:g.73993449_73993450dup	NC_000002.11:g.73993448_73993450dup	NC_000002.11:g.73993447_73993450dup	NC_000002.11:g.73993443_73993450dup
GRCh38.p14 chr 2 fix patch HG2052_PATCH	NW_025791766.1:g.435808_435821=	NW_025791766.1:g.435819_435821del	NW_025791766.1:g.435820_435821del	NW_025791766.1:g.435821del	NW_025791766.1:g.435821dup	NW_025791766.1:g.435820_435821dup	NW_025791766.1:g.435819_435821dup	NW_025791766.1:g.435818_435821dup	NW_025791766.1:g.435814_435821dup
DUSP11 transcript	NM_003584.2:c.935+108=	NM_003584.2:c.935+106_935+108del	NM_003584.2:c.935+107_935+108del	NM_003584.2:c.935+108del	NM_003584.2:c.935+108dup	NM_003584.2:c.935+107_935+108dup	NM_003584.2:c.935+106_935+108dup	NM_003584.2:c.935+105_935+108dup	NM_003584.2:c.935+101_935+108dup
DUSP11 transcript variant 1	NM_003584.3:c.794+108=	NM_003584.3:c.794+106_794+108del	NM_003584.3:c.794+107_794+108del	NM_003584.3:c.794+108del	NM_003584.3:c.794+108dup	NM_003584.3:c.794+107_794+108dup	NM_003584.3:c.794+106_794+108dup	NM_003584.3:c.794+105_794+108dup	NM_003584.3:c.794+101_794+108dup

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, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41642651	Dec 03, 2013 (138)
2	HGSV	ss80219835	Sep 08, 2015 (146)
3	HGSV	ss82240957	Sep 08, 2015 (146)
4	HGSV	ss82298373	Sep 08, 2015 (146)
5	HGSV	ss82321875	Sep 08, 2015 (146)
6	HUMANGENOME_JCVI	ss95276671	Dec 05, 2013 (138)
7	GMI	ss288179667	May 04, 2012 (137)
8	GMI	ss288179669	May 04, 2012 (137)
9	PJP	ss294989944	May 09, 2011 (137)
10	PJP	ss294989945	May 09, 2011 (134)
11	SSMP	ss663325705	Apr 01, 2015 (144)
12	1000GENOMES	ss1368337920	Aug 21, 2014 (142)
13	1000GENOMES	ss1368337921	Aug 21, 2014 (142)
14	EVA_GENOME_DK	ss1575437347	Apr 01, 2015 (144)
15	JJLAB	ss2030421711	Sep 14, 2016 (149)
16	SWEGEN	ss2989748083	Nov 08, 2017 (151)
17	URBANLAB	ss3647064234	Oct 11, 2018 (152)
18	EVA_DECODE	ss3704188950	Jul 13, 2019 (153)
19	EVA_DECODE	ss3704188951	Jul 13, 2019 (153)
20	EVA_DECODE	ss3704188952	Jul 13, 2019 (153)
21	EVA_DECODE	ss3704188953	Jul 13, 2019 (153)
22	ACPOP	ss3728561074	Jul 13, 2019 (153)
23	PACBIO	ss3783899665	Jul 13, 2019 (153)
24	PACBIO	ss3789480053	Jul 13, 2019 (153)
25	PACBIO	ss3794353017	Jul 13, 2019 (153)
26	KHV_HUMAN_GENOMES	ss3801311450	Jul 13, 2019 (153)
27	EVA	ss3827054562	Apr 25, 2020 (154)
28	EVA	ss3836936515	Apr 25, 2020 (154)
29	EVA	ss3842352664	Apr 25, 2020 (154)
30	KOGIC	ss3948051850	Apr 25, 2020 (154)
31	KOGIC	ss3948051851	Apr 25, 2020 (154)
32	KOGIC	ss3948051852	Apr 25, 2020 (154)
33	FSA-LAB	ss3984179835	Apr 26, 2021 (155)
34	EVA	ss3986185580	Apr 26, 2021 (155)
35	GNOMAD	ss4044005521	Apr 26, 2021 (155)
36	GNOMAD	ss4044005522	Apr 26, 2021 (155)
37	GNOMAD	ss4044005523	Apr 26, 2021 (155)
38	GNOMAD	ss4044005524	Apr 26, 2021 (155)
39	GNOMAD	ss4044005525	Apr 26, 2021 (155)
40	GNOMAD	ss4044005526	Apr 26, 2021 (155)
41	EVA	ss5141889176	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5152052994	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5152052995	Apr 26, 2021 (155)
44	EVA	ss5237169919	Apr 26, 2021 (155)
45	1000G_HIGH_COVERAGE	ss5248588405	Oct 12, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5248588406	Oct 12, 2022 (156)
47	1000G_HIGH_COVERAGE	ss5248588407	Oct 12, 2022 (156)
48	HUGCELL_USP	ss5448741452	Oct 12, 2022 (156)
49	HUGCELL_USP	ss5448741453	Oct 12, 2022 (156)
50	HUGCELL_USP	ss5448741454	Oct 12, 2022 (156)
51	HUGCELL_USP	ss5448741455	Oct 12, 2022 (156)
52	EVA	ss5624100393	Oct 12, 2022 (156)
53	TOMMO_GENOMICS	ss5680876623	Oct 12, 2022 (156)
54	TOMMO_GENOMICS	ss5680876624	Oct 12, 2022 (156)
55	EVA	ss5820300808	Oct 12, 2022 (156)
56	EVA	ss5852579794	Oct 12, 2022 (156)
57	EVA	ss5930977457	Oct 12, 2022 (156)
58	EVA	ss5980063720	Oct 12, 2022 (156)
59	1000Genomes	NC_000002.11 - 73993437	Oct 11, 2018 (152)
60	The Danish reference pan genome	NC_000002.11 - 73993437	Apr 25, 2020 (154)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62628959 (NC_000002.12:73766309::A 293/115770) Row 62628960 (NC_000002.12:73766309::AA 5/115850) Row 62628961 (NC_000002.12:73766309::AAA 1/115852)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62628959 (NC_000002.12:73766309::A 293/115770) Row 62628960 (NC_000002.12:73766309::AA 5/115850) Row 62628961 (NC_000002.12:73766309::AAA 1/115852)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62628959 (NC_000002.12:73766309::A 293/115770) Row 62628960 (NC_000002.12:73766309::AA 5/115850) Row 62628961 (NC_000002.12:73766309::AAA 1/115852)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62628959 (NC_000002.12:73766309::A 293/115770) Row 62628960 (NC_000002.12:73766309::AA 5/115850) Row 62628961 (NC_000002.12:73766309::AAA 1/115852)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62628959 (NC_000002.12:73766309::A 293/115770) Row 62628960 (NC_000002.12:73766309::AA 5/115850) Row 62628961 (NC_000002.12:73766309::AAA 1/115852)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62628959 (NC_000002.12:73766309::A 293/115770) Row 62628960 (NC_000002.12:73766309::AA 5/115850) Row 62628961 (NC_000002.12:73766309::AAA 1/115852)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62628959 (NC_000002.12:73766309::A 293/115770) Row 62628960 (NC_000002.12:73766309::AA 5/115850) Row 62628961 (NC_000002.12:73766309::AAA 1/115852)...	-	Apr 26, 2021 (155)
68	Korean Genome Project Submission ignored due to conflicting rows: Row 4429851 (NC_000002.12:73766310:A: 1081/1832) Row 4429852 (NC_000002.12:73766309:AA: 27/1832) Row 4429853 (NC_000002.12:73766311::A 24/1832)	-	Apr 25, 2020 (154)
69	Korean Genome Project Submission ignored due to conflicting rows: Row 4429851 (NC_000002.12:73766310:A: 1081/1832) Row 4429852 (NC_000002.12:73766309:AA: 27/1832) Row 4429853 (NC_000002.12:73766311::A 24/1832)	-	Apr 25, 2020 (154)
70	Korean Genome Project Submission ignored due to conflicting rows: Row 4429851 (NC_000002.12:73766310:A: 1081/1832) Row 4429852 (NC_000002.12:73766309:AA: 27/1832) Row 4429853 (NC_000002.12:73766311::A 24/1832)	-	Apr 25, 2020 (154)
71	Northern Sweden	NC_000002.11 - 73993437	Jul 13, 2019 (153)
72	8.3KJPN Submission ignored due to conflicting rows: Row 10022301 (NC_000002.11:73993436:A: 10691/16760) Row 10022302 (NC_000002.11:73993436::A 12/16760)	-	Apr 26, 2021 (155)
73	8.3KJPN Submission ignored due to conflicting rows: Row 10022301 (NC_000002.11:73993436:A: 10691/16760) Row 10022302 (NC_000002.11:73993436::A 12/16760)	-	Apr 26, 2021 (155)
74	14KJPN Submission ignored due to conflicting rows: Row 14713727 (NC_000002.12:73766309:A: 17877/28258) Row 14713728 (NC_000002.12:73766309::A 19/28258)	-	Oct 12, 2022 (156)
75	14KJPN Submission ignored due to conflicting rows: Row 14713727 (NC_000002.12:73766309:A: 17877/28258) Row 14713728 (NC_000002.12:73766309::A 19/28258)	-	Oct 12, 2022 (156)
76	ALFA	NC_000002.12 - 73766310	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)
rs56916698	May 23, 2008 (130)
rs71838809	May 11, 2012 (137)
rs146956468	May 11, 2012 (137)
rs370215907	May 13, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
8818706, ss1368337920	NC_000002.11:73993436:AAA:	NC_000002.12:73766309:AAAAAAAAAAAA… NC_000002.12:73766309:AAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4044005526	NC_000002.12:73766309:AAA:	NC_000002.12:73766309:AAAAAAAAAAAA… NC_000002.12:73766309:AAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss288179669	NC_000002.10:73846944:AA:	NC_000002.12:73766309:AAAAAAAAAAAA… NC_000002.12:73766309:AAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3984179835	NC_000002.11:73993436:AA:	NC_000002.12:73766309:AAAAAAAAAAAA… NC_000002.12:73766309:AAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3704188953, ss3948051851, ss4044005525, ss5248588406, ss5448741455	NC_000002.12:73766309:AA:	NC_000002.12:73766309:AAAAAAAAAAAA… NC_000002.12:73766309:AAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
1997755074	NC_000002.12:73766309:AAAAAAAAAAAA… NC_000002.12:73766309:AAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000002.12:73766309:AAAAAAAAAAAA… NC_000002.12:73766309:AAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss80219835, ss82240957, ss82298373, ss82321875	NC_000002.9:73905104:A:	NC_000002.12:73766309:AAAAAAAAAAAA… NC_000002.12:73766309:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss288179667, ss294989944	NC_000002.10:73846944:A:	NC_000002.12:73766309:AAAAAAAAAAAA… NC_000002.12:73766309:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss294989945	NC_000002.10:73846957:A:	NC_000002.12:73766309:AAAAAAAAAAAA… NC_000002.12:73766309:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
675706, 1845939, ss663325705, ss1575437347, ss2030421711, ss2989748083, ss3728561074, ss3783899665, ss3789480053, ss3794353017, ss3827054562, ss3836936515, ss3986185580, ss5152052994, ss5624100393, ss5820300808, ss5980063720	NC_000002.11:73993436:A:	NC_000002.12:73766309:AAAAAAAAAAAA… NC_000002.12:73766309:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss1368337921	NC_000002.11:73993438:A:	NC_000002.12:73766309:AAAAAAAAAAAA… NC_000002.12:73766309:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3647064234, ss3842352664, ss5237169919, ss5248588405, ss5448741452, ss5680876623, ss5852579794, ss5930977457	NC_000002.12:73766309:A:	NC_000002.12:73766309:AAAAAAAAAAAA… NC_000002.12:73766309:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
1997755074	NC_000002.12:73766309:AAAAAAAAAAAA… NC_000002.12:73766309:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000002.12:73766309:AAAAAAAAAAAA… NC_000002.12:73766309:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3704188952, ss3948051850	NC_000002.12:73766310:A:	NC_000002.12:73766309:AAAAAAAAAAAA… NC_000002.12:73766309:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3801311450	NC_000002.12:73766311:A:	NC_000002.12:73766309:AAAAAAAAAAAA… NC_000002.12:73766309:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss41642651, ss95276671	NT_022184.15:52815336:A:	NC_000002.12:73766309:AAAAAAAAAAAA… NC_000002.12:73766309:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss5152052995	NC_000002.11:73993436::A	NC_000002.12:73766309:AAAAAAAAAAAA… NC_000002.12:73766309:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4044005521, ss5141889176, ss5248588407, ss5448741453, ss5680876624	NC_000002.12:73766309::A	NC_000002.12:73766309:AAAAAAAAAAAA… NC_000002.12:73766309:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
1997755074	NC_000002.12:73766309:AAAAAAAAAAAA… NC_000002.12:73766309:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000002.12:73766309:AAAAAAAAAAAA… NC_000002.12:73766309:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3704188951, ss3948051852	NC_000002.12:73766311::A	NC_000002.12:73766309:AAAAAAAAAAAA… NC_000002.12:73766309:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4044005522, ss5448741454	NC_000002.12:73766309::AA	NC_000002.12:73766309:AAAAAAAAAAAA… NC_000002.12:73766309:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
1997755074	NC_000002.12:73766309:AAAAAAAAAAAA… NC_000002.12:73766309:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000002.12:73766309:AAAAAAAAAAAA… NC_000002.12:73766309:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4044005523	NC_000002.12:73766309::AAA	NC_000002.12:73766309:AAAAAAAAAAAA… NC_000002.12:73766309:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4044005524	NC_000002.12:73766309::AAAA	NC_000002.12:73766309:AAAAAAAAAAAA… NC_000002.12:73766309:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3704188950	NC_000002.12:73766311::AAAAAAAA	NC_000002.12:73766309:AAAAAAAAAAAA… NC_000002.12:73766309:AAAAAAAAAAAAAA: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 rs34279043

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

rs34279043