Name: rs34561776
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.

rs34561776

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:17039416-17039437 (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)₁₁ / del(A)₉ / del(A)₇ / del…
del(A)₁₁ / del(A)₉ / del(A)₇ / del(A)₆ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₉=0.000008 (2/264690, TOPMED)
del(A)₁₁=0.0000 (0/2626, ALFA)
del(A)₉=0.0000 (0/2626, ALFA) (+ 7 more)
del(A)₇=0.0000 (0/2626, ALFA)
del(A)₆=0.0000 (0/2626, ALFA)
delAAA=0.0000 (0/2626, ALFA)
delA=0.0000 (0/2626, ALFA)
dupA=0.0000 (0/2626, ALFA)
dupAA=0.0000 (0/2626, ALFA)
dup(A)₄=0.0000 (0/2626, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SDHB : 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	2626	AAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	1418	AAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	832	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	42	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	790	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	58	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	38	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	20	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	40	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	128	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	30	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	120	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	(A)₂₂=0.999992	del(A)₉=0.000008
Allele Frequency Aggregator	Total	Global	2626	(A)₂₂=1.0000	del(A)₁₁=0.0000, del(A)₉=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, delAAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	European	Sub	1418	(A)₂₂=1.0000	del(A)₁₁=0.0000, del(A)₉=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, delAAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	African	Sub	832	(A)₂₂=1.000	del(A)₁₁=0.000, del(A)₉=0.000, del(A)₇=0.000, del(A)₆=0.000, delAAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Latin American 2	Sub	128	(A)₂₂=1.000	del(A)₁₁=0.000, del(A)₉=0.000, del(A)₇=0.000, del(A)₆=0.000, delAAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Other	Sub	120	(A)₂₂=1.000	del(A)₁₁=0.000, del(A)₉=0.000, del(A)₇=0.000, del(A)₆=0.000, delAAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Asian	Sub	58	(A)₂₂=1.00	del(A)₁₁=0.00, del(A)₉=0.00, del(A)₇=0.00, del(A)₆=0.00, delAAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	Latin American 1	Sub	40	(A)₂₂=1.00	del(A)₁₁=0.00, del(A)₉=0.00, del(A)₇=0.00, del(A)₆=0.00, delAAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	30	(A)₂₂=1.00	del(A)₁₁=0.00, del(A)₉=0.00, del(A)₇=0.00, del(A)₆=0.00, delAAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dup(A)₄=0.00

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.17039427_17039437del
GRCh38.p14 chr 1	NC_000001.11:g.17039429_17039437del
GRCh38.p14 chr 1	NC_000001.11:g.17039431_17039437del
GRCh38.p14 chr 1	NC_000001.11:g.17039432_17039437del
GRCh38.p14 chr 1	NC_000001.11:g.17039435_17039437del
GRCh38.p14 chr 1	NC_000001.11:g.17039436_17039437del
GRCh38.p14 chr 1	NC_000001.11:g.17039437del
GRCh38.p14 chr 1	NC_000001.11:g.17039437dup
GRCh38.p14 chr 1	NC_000001.11:g.17039436_17039437dup
GRCh38.p14 chr 1	NC_000001.11:g.17039435_17039437dup
GRCh38.p14 chr 1	NC_000001.11:g.17039434_17039437dup
GRCh38.p14 chr 1	NC_000001.11:g.17039433_17039437dup
GRCh38.p14 chr 1	NC_000001.11:g.17039432_17039437dup
GRCh37.p13 chr 1	NC_000001.10:g.17365922_17365932del
GRCh37.p13 chr 1	NC_000001.10:g.17365924_17365932del
GRCh37.p13 chr 1	NC_000001.10:g.17365926_17365932del
GRCh37.p13 chr 1	NC_000001.10:g.17365927_17365932del
GRCh37.p13 chr 1	NC_000001.10:g.17365930_17365932del
GRCh37.p13 chr 1	NC_000001.10:g.17365931_17365932del
GRCh37.p13 chr 1	NC_000001.10:g.17365932del
GRCh37.p13 chr 1	NC_000001.10:g.17365932dup
GRCh37.p13 chr 1	NC_000001.10:g.17365931_17365932dup
GRCh37.p13 chr 1	NC_000001.10:g.17365930_17365932dup
GRCh37.p13 chr 1	NC_000001.10:g.17365929_17365932dup
GRCh37.p13 chr 1	NC_000001.10:g.17365928_17365932dup
GRCh37.p13 chr 1	NC_000001.10:g.17365927_17365932dup
SDHB RefSeqGene (LRG_316)	NG_012340.1:g.19745_19755del
SDHB RefSeqGene (LRG_316)	NG_012340.1:g.19747_19755del
SDHB RefSeqGene (LRG_316)	NG_012340.1:g.19749_19755del
SDHB RefSeqGene (LRG_316)	NG_012340.1:g.19750_19755del
SDHB RefSeqGene (LRG_316)	NG_012340.1:g.19753_19755del
SDHB RefSeqGene (LRG_316)	NG_012340.1:g.19754_19755del
SDHB RefSeqGene (LRG_316)	NG_012340.1:g.19755del
SDHB RefSeqGene (LRG_316)	NG_012340.1:g.19755dup
SDHB RefSeqGene (LRG_316)	NG_012340.1:g.19754_19755dup
SDHB RefSeqGene (LRG_316)	NG_012340.1:g.19753_19755dup
SDHB RefSeqGene (LRG_316)	NG_012340.1:g.19752_19755dup
SDHB RefSeqGene (LRG_316)	NG_012340.1:g.19751_19755dup
SDHB RefSeqGene (LRG_316)	NG_012340.1:g.19750_19755dup
GRCh38.p14 chr 1 fix patch HG1343_HG173_HG459_PATCH	NW_025791756.1:g.1454620_1454630del
GRCh38.p14 chr 1 fix patch HG1343_HG173_HG459_PATCH	NW_025791756.1:g.1454622_1454630del
GRCh38.p14 chr 1 fix patch HG1343_HG173_HG459_PATCH	NW_025791756.1:g.1454624_1454630del
GRCh38.p14 chr 1 fix patch HG1343_HG173_HG459_PATCH	NW_025791756.1:g.1454625_1454630del
GRCh38.p14 chr 1 fix patch HG1343_HG173_HG459_PATCH	NW_025791756.1:g.1454628_1454630del
GRCh38.p14 chr 1 fix patch HG1343_HG173_HG459_PATCH	NW_025791756.1:g.1454629_1454630del
GRCh38.p14 chr 1 fix patch HG1343_HG173_HG459_PATCH	NW_025791756.1:g.1454630del
GRCh38.p14 chr 1 fix patch HG1343_HG173_HG459_PATCH	NW_025791756.1:g.1454630dup
GRCh38.p14 chr 1 fix patch HG1343_HG173_HG459_PATCH	NW_025791756.1:g.1454629_1454630dup
GRCh38.p14 chr 1 fix patch HG1343_HG173_HG459_PATCH	NW_025791756.1:g.1454628_1454630dup
GRCh38.p14 chr 1 fix patch HG1343_HG173_HG459_PATCH	NW_025791756.1:g.1454627_1454630dup
GRCh38.p14 chr 1 fix patch HG1343_HG173_HG459_PATCH	NW_025791756.1:g.1454626_1454630dup
GRCh38.p14 chr 1 fix patch HG1343_HG173_HG459_PATCH	NW_025791756.1:g.1454625_1454630dup

Gene: SDHB, succinate dehydrogenase complex iron sulfur subunit B (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SDHB transcript variant 1	NM_003000.3:c.200+5335_20… NM_003000.3:c.200+5335_200+5345del	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)₂₂=	del(A)₁₁	del(A)₉	del(A)₇	del(A)₆	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆
GRCh38.p14 chr 1	NC_000001.11:g.17039416_17039437=	NC_000001.11:g.17039427_17039437del	NC_000001.11:g.17039429_17039437del	NC_000001.11:g.17039431_17039437del	NC_000001.11:g.17039432_17039437del	NC_000001.11:g.17039435_17039437del	NC_000001.11:g.17039436_17039437del	NC_000001.11:g.17039437del	NC_000001.11:g.17039437dup	NC_000001.11:g.17039436_17039437dup	NC_000001.11:g.17039435_17039437dup	NC_000001.11:g.17039434_17039437dup	NC_000001.11:g.17039433_17039437dup	NC_000001.11:g.17039432_17039437dup
GRCh37.p13 chr 1	NC_000001.10:g.17365911_17365932=	NC_000001.10:g.17365922_17365932del	NC_000001.10:g.17365924_17365932del	NC_000001.10:g.17365926_17365932del	NC_000001.10:g.17365927_17365932del	NC_000001.10:g.17365930_17365932del	NC_000001.10:g.17365931_17365932del	NC_000001.10:g.17365932del	NC_000001.10:g.17365932dup	NC_000001.10:g.17365931_17365932dup	NC_000001.10:g.17365930_17365932dup	NC_000001.10:g.17365929_17365932dup	NC_000001.10:g.17365928_17365932dup	NC_000001.10:g.17365927_17365932dup
SDHB RefSeqGene (LRG_316)	NG_012340.1:g.19734_19755=	NG_012340.1:g.19745_19755del	NG_012340.1:g.19747_19755del	NG_012340.1:g.19749_19755del	NG_012340.1:g.19750_19755del	NG_012340.1:g.19753_19755del	NG_012340.1:g.19754_19755del	NG_012340.1:g.19755del	NG_012340.1:g.19755dup	NG_012340.1:g.19754_19755dup	NG_012340.1:g.19753_19755dup	NG_012340.1:g.19752_19755dup	NG_012340.1:g.19751_19755dup	NG_012340.1:g.19750_19755dup
GRCh38.p14 chr 1 fix patch HG1343_HG173_HG459_PATCH	NW_025791756.1:g.1454608_1454630=	NW_025791756.1:g.1454620_1454630del	NW_025791756.1:g.1454622_1454630del	NW_025791756.1:g.1454624_1454630del	NW_025791756.1:g.1454625_1454630del	NW_025791756.1:g.1454628_1454630del	NW_025791756.1:g.1454629_1454630del	NW_025791756.1:g.1454630del	NW_025791756.1:g.1454630dup	NW_025791756.1:g.1454629_1454630dup	NW_025791756.1:g.1454628_1454630dup	NW_025791756.1:g.1454627_1454630dup	NW_025791756.1:g.1454626_1454630dup	NW_025791756.1:g.1454625_1454630dup
SDHB transcript	NM_003000.2:c.200+5345=	NM_003000.2:c.200+5335_200+5345del	NM_003000.2:c.200+5337_200+5345del	NM_003000.2:c.200+5339_200+5345del	NM_003000.2:c.200+5340_200+5345del	NM_003000.2:c.200+5343_200+5345del	NM_003000.2:c.200+5344_200+5345del	NM_003000.2:c.200+5345del	NM_003000.2:c.200+5345dup	NM_003000.2:c.200+5344_200+5345dup	NM_003000.2:c.200+5343_200+5345dup	NM_003000.2:c.200+5342_200+5345dup	NM_003000.2:c.200+5341_200+5345dup	NM_003000.2:c.200+5340_200+5345dup
SDHB transcript variant 1	NM_003000.3:c.200+5345=	NM_003000.3:c.200+5335_200+5345del	NM_003000.3:c.200+5337_200+5345del	NM_003000.3:c.200+5339_200+5345del	NM_003000.3:c.200+5340_200+5345del	NM_003000.3:c.200+5343_200+5345del	NM_003000.3:c.200+5344_200+5345del	NM_003000.3:c.200+5345del	NM_003000.3:c.200+5345dup	NM_003000.3:c.200+5344_200+5345dup	NM_003000.3:c.200+5343_200+5345dup	NM_003000.3:c.200+5342_200+5345dup	NM_003000.3:c.200+5341_200+5345dup	NM_003000.3:c.200+5340_200+5345dup

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#.

38 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41208129	Mar 14, 2006 (126)
2	PJP	ss294567639	May 09, 2011 (134)
3	SWEGEN	ss2986388675	Nov 08, 2017 (151)
4	SWEGEN	ss2986388676	Nov 08, 2017 (151)
5	SWEGEN	ss2986388677	Nov 08, 2017 (151)
6	EVA_DECODE	ss3686248620	Jul 12, 2019 (153)
7	EVA_DECODE	ss3686248621	Jul 12, 2019 (153)
8	EVA_DECODE	ss3686248622	Jul 12, 2019 (153)
9	PACBIO	ss3789010770	Jul 12, 2019 (153)
10	PACBIO	ss3793883227	Jul 12, 2019 (153)
11	EVA	ss3826044654	Apr 25, 2020 (154)
12	GNOMAD	ss3989050351	Apr 27, 2021 (155)
13	GNOMAD	ss3989050352	Apr 27, 2021 (155)
14	GNOMAD	ss3989050353	Apr 27, 2021 (155)
15	GNOMAD	ss3989050354	Apr 27, 2021 (155)
16	GNOMAD	ss3989050355	Apr 27, 2021 (155)
17	GNOMAD	ss3989050356	Apr 27, 2021 (155)
18	GNOMAD	ss3989050357	Apr 27, 2021 (155)
19	GNOMAD	ss3989050358	Apr 27, 2021 (155)
20	GNOMAD	ss3989050359	Apr 27, 2021 (155)
21	GNOMAD	ss3989050360	Apr 27, 2021 (155)
22	GNOMAD	ss3989050361	Apr 27, 2021 (155)
23	GNOMAD	ss3989050362	Apr 27, 2021 (155)
24	TOPMED	ss4440556514	Apr 27, 2021 (155)
25	TOMMO_GENOMICS	ss5142710332	Apr 27, 2021 (155)
26	TOMMO_GENOMICS	ss5142710333	Apr 27, 2021 (155)
27	TOMMO_GENOMICS	ss5142710334	Apr 27, 2021 (155)
28	1000G_HIGH_COVERAGE	ss5241341294	Oct 12, 2022 (156)
29	1000G_HIGH_COVERAGE	ss5241341295	Oct 12, 2022 (156)
30	1000G_HIGH_COVERAGE	ss5241341296	Oct 12, 2022 (156)
31	HUGCELL_USP	ss5442506953	Oct 12, 2022 (156)
32	HUGCELL_USP	ss5442506954	Oct 12, 2022 (156)
33	HUGCELL_USP	ss5442506955	Oct 12, 2022 (156)
34	SANFORD_IMAGENETICS	ss5625019033	Oct 12, 2022 (156)
35	TOMMO_GENOMICS	ss5667081110	Oct 12, 2022 (156)
36	TOMMO_GENOMICS	ss5667081112	Oct 12, 2022 (156)
37	TOMMO_GENOMICS	ss5667081113	Oct 12, 2022 (156)
38	EVA	ss5848801564	Oct 12, 2022 (156)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3714167 (NC_000001.11:17039415::A 49786/79388) Row 3714168 (NC_000001.11:17039415::AA 1189/78962) Row 3714169 (NC_000001.11:17039415::AAA 22/78942)...	-	Apr 27, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3714167 (NC_000001.11:17039415::A 49786/79388) Row 3714168 (NC_000001.11:17039415::AA 1189/78962) Row 3714169 (NC_000001.11:17039415::AAA 22/78942)...	-	Apr 27, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3714167 (NC_000001.11:17039415::A 49786/79388) Row 3714168 (NC_000001.11:17039415::AA 1189/78962) Row 3714169 (NC_000001.11:17039415::AAA 22/78942)...	-	Apr 27, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3714167 (NC_000001.11:17039415::A 49786/79388) Row 3714168 (NC_000001.11:17039415::AA 1189/78962) Row 3714169 (NC_000001.11:17039415::AAA 22/78942)...	-	Apr 27, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3714167 (NC_000001.11:17039415::A 49786/79388) Row 3714168 (NC_000001.11:17039415::AA 1189/78962) Row 3714169 (NC_000001.11:17039415::AAA 22/78942)...	-	Apr 27, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3714167 (NC_000001.11:17039415::A 49786/79388) Row 3714168 (NC_000001.11:17039415::AA 1189/78962) Row 3714169 (NC_000001.11:17039415::AAA 22/78942)...	-	Apr 27, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3714167 (NC_000001.11:17039415::A 49786/79388) Row 3714168 (NC_000001.11:17039415::AA 1189/78962) Row 3714169 (NC_000001.11:17039415::AAA 22/78942)...	-	Apr 27, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3714167 (NC_000001.11:17039415::A 49786/79388) Row 3714168 (NC_000001.11:17039415::AA 1189/78962) Row 3714169 (NC_000001.11:17039415::AAA 22/78942)...	-	Apr 27, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3714167 (NC_000001.11:17039415::A 49786/79388) Row 3714168 (NC_000001.11:17039415::AA 1189/78962) Row 3714169 (NC_000001.11:17039415::AAA 22/78942)...	-	Apr 27, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3714167 (NC_000001.11:17039415::A 49786/79388) Row 3714168 (NC_000001.11:17039415::AA 1189/78962) Row 3714169 (NC_000001.11:17039415::AAA 22/78942)...	-	Apr 27, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3714167 (NC_000001.11:17039415::A 49786/79388) Row 3714168 (NC_000001.11:17039415::AA 1189/78962) Row 3714169 (NC_000001.11:17039415::AAA 22/78942)...	-	Apr 27, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3714167 (NC_000001.11:17039415::A 49786/79388) Row 3714168 (NC_000001.11:17039415::AA 1189/78962) Row 3714169 (NC_000001.11:17039415::AAA 22/78942)...	-	Apr 27, 2021 (155)
51	8.3KJPN Submission ignored due to conflicting rows: Row 679639 (NC_000001.10:17365910::A 4267/16442) Row 679640 (NC_000001.10:17365910::AA 50/16442) Row 679641 (NC_000001.10:17365910::AAAA 5/16442)	-	Apr 27, 2021 (155)
52	8.3KJPN Submission ignored due to conflicting rows: Row 679639 (NC_000001.10:17365910::A 4267/16442) Row 679640 (NC_000001.10:17365910::AA 50/16442) Row 679641 (NC_000001.10:17365910::AAAA 5/16442)	-	Apr 27, 2021 (155)
53	8.3KJPN Submission ignored due to conflicting rows: Row 679639 (NC_000001.10:17365910::A 4267/16442) Row 679640 (NC_000001.10:17365910::AA 50/16442) Row 679641 (NC_000001.10:17365910::AAAA 5/16442)	-	Apr 27, 2021 (155)
54	14KJPN Submission ignored due to conflicting rows: Row 918214 (NC_000001.11:17039415::A 7579/28010) Row 918216 (NC_000001.11:17039415::AAAA 4/28010) Row 918217 (NC_000001.11:17039415::AA 69/28010)	-	Oct 12, 2022 (156)
55	14KJPN Submission ignored due to conflicting rows: Row 918214 (NC_000001.11:17039415::A 7579/28010) Row 918216 (NC_000001.11:17039415::AAAA 4/28010) Row 918217 (NC_000001.11:17039415::AA 69/28010)	-	Oct 12, 2022 (156)
56	14KJPN Submission ignored due to conflicting rows: Row 918214 (NC_000001.11:17039415::A 7579/28010) Row 918216 (NC_000001.11:17039415::AAAA 4/28010) Row 918217 (NC_000001.11:17039415::AA 69/28010)	-	Oct 12, 2022 (156)
57	TopMed	NC_000001.11 - 17039416	Apr 27, 2021 (155)
58	ALFA	NC_000001.11 - 17039416	Apr 27, 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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3989050362	NC_000001.11:17039415:AAAAAAAAAAA:	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
10715676677	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
4162849, ss3989050361, ss4440556514	NC_000001.11:17039415:AAAAAAAAA:	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
10715676677	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3989050360	NC_000001.11:17039415:AAAAAAA:	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
10715676677	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
10715676677	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3989050359	NC_000001.11:17039415:AAA:	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
10715676677	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3989050358	NC_000001.11:17039415:AA:	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3686248622, ss3989050357, ss5241341295, ss5442506955	NC_000001.11:17039415:A:	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
10715676677	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss294567639	NC_000001.9:17238519::A	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss2986388675, ss3789010770, ss3793883227, ss3826044654, ss5142710332, ss5625019033	NC_000001.10:17365910::A	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3989050351, ss5241341294, ss5442506953, ss5667081110, ss5848801564	NC_000001.11:17039415::A	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
10715676677	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3686248621	NC_000001.11:17039416::A	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss41208129	NT_004610.19:4045998::A	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss2986388677, ss5142710333	NC_000001.10:17365910::AA	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3989050352, ss5241341296, ss5442506954, ss5667081113	NC_000001.11:17039415::AA	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
10715676677	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3686248620	NC_000001.11:17039416::AA	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3989050353	NC_000001.11:17039415::AAA	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss2986388676, ss5142710334	NC_000001.10:17365910::AAAA	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3989050354, ss5667081112	NC_000001.11:17039415::AAAA	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
10715676677	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3989050355	NC_000001.11:17039415::AAAAA	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3989050356	NC_000001.11:17039415::AAAAAA	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3069733781	NC_000001.11:17039415:AAAAAA:	NC_000001.11:17039415:AAAAAAAAAAAA… NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs34561776

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

rs34561776