Name: rs34130331
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.

rs34130331

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr19:3957996-3958017 (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)₁₂ / del(A)₁₁ / del(A)₁₀ / d…
del(A)₁₂ / del(A)₁₁ / del(A)₁₀ / del(A)₉ / del(A)₈ / del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₂=0.0000 (0/1142, ALFA)
del(A)₁₁=0.0000 (0/1142, ALFA)
del(A)₁₀=0.0000 (0/1142, ALFA) (+ 14 more)
del(A)₉=0.0000 (0/1142, ALFA)
del(A)₈=0.0000 (0/1142, ALFA)
del(A)₇=0.0000 (0/1142, ALFA)
del(A)₆=0.0000 (0/1142, ALFA)
del(A)₅=0.0000 (0/1142, ALFA)
del(A)₄=0.0000 (0/1142, ALFA)
delAAA=0.0000 (0/1142, ALFA)
delAA=0.0000 (0/1142, ALFA)
delA=0.0000 (0/1142, ALFA)
dupA=0.0000 (0/1142, ALFA)
dupAA=0.0000 (0/1142, ALFA)
dupAAA=0.0000 (0/1142, ALFA)
dup(A)₄=0.0000 (0/1142, ALFA)
dup(A)₅=0.0000 (0/1142, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: DAPK3 : 500B Downstream 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	1142	AAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
European	Sub	464	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African	Sub	612	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	32	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	580	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	2	AAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	2	AAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	12	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	14	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	6	AAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other	Sub	32	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	1142	(A)₂₂=1.0000	del(A)₁₂=0.0000, del(A)₁₁=0.0000, del(A)₁₀=0.0000, del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000
Allele Frequency Aggregator	African	Sub	612	(A)₂₂=1.000	del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	European	Sub	464	(A)₂₂=1.000	del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Other	Sub	32	(A)₂₂=1.00	del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	Latin American 2	Sub	14	(A)₂₂=1.00	del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	Latin American 1	Sub	12	(A)₂₂=1.00	del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	6	(A)₂₂=1.0	del(A)₁₂=0.0, del(A)₁₁=0.0, del(A)₁₀=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₆=0.0, del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0, dup(A)₅=0.0
Allele Frequency Aggregator	Asian	Sub	2	(A)₂₂=1.0	del(A)₁₂=0.0, del(A)₁₁=0.0, del(A)₁₀=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₆=0.0, del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0, dup(A)₅=0.0

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 19	NC_000019.10:g.3958006_3958017del
GRCh38.p14 chr 19	NC_000019.10:g.3958007_3958017del
GRCh38.p14 chr 19	NC_000019.10:g.3958008_3958017del
GRCh38.p14 chr 19	NC_000019.10:g.3958009_3958017del
GRCh38.p14 chr 19	NC_000019.10:g.3958010_3958017del
GRCh38.p14 chr 19	NC_000019.10:g.3958011_3958017del
GRCh38.p14 chr 19	NC_000019.10:g.3958012_3958017del
GRCh38.p14 chr 19	NC_000019.10:g.3958013_3958017del
GRCh38.p14 chr 19	NC_000019.10:g.3958014_3958017del
GRCh38.p14 chr 19	NC_000019.10:g.3958015_3958017del
GRCh38.p14 chr 19	NC_000019.10:g.3958016_3958017del
GRCh38.p14 chr 19	NC_000019.10:g.3958017del
GRCh38.p14 chr 19	NC_000019.10:g.3958017dup
GRCh38.p14 chr 19	NC_000019.10:g.3958016_3958017dup
GRCh38.p14 chr 19	NC_000019.10:g.3958015_3958017dup
GRCh38.p14 chr 19	NC_000019.10:g.3958014_3958017dup
GRCh38.p14 chr 19	NC_000019.10:g.3958013_3958017dup
GRCh38.p14 chr 19	NC_000019.10:g.3958012_3958017dup
GRCh37.p13 chr 19	NC_000019.9:g.3958004_3958015del
GRCh37.p13 chr 19	NC_000019.9:g.3958005_3958015del
GRCh37.p13 chr 19	NC_000019.9:g.3958006_3958015del
GRCh37.p13 chr 19	NC_000019.9:g.3958007_3958015del
GRCh37.p13 chr 19	NC_000019.9:g.3958008_3958015del
GRCh37.p13 chr 19	NC_000019.9:g.3958009_3958015del
GRCh37.p13 chr 19	NC_000019.9:g.3958010_3958015del
GRCh37.p13 chr 19	NC_000019.9:g.3958011_3958015del
GRCh37.p13 chr 19	NC_000019.9:g.3958012_3958015del
GRCh37.p13 chr 19	NC_000019.9:g.3958013_3958015del
GRCh37.p13 chr 19	NC_000019.9:g.3958014_3958015del
GRCh37.p13 chr 19	NC_000019.9:g.3958015del
GRCh37.p13 chr 19	NC_000019.9:g.3958015dup
GRCh37.p13 chr 19	NC_000019.9:g.3958014_3958015dup
GRCh37.p13 chr 19	NC_000019.9:g.3958013_3958015dup
GRCh37.p13 chr 19	NC_000019.9:g.3958012_3958015dup
GRCh37.p13 chr 19	NC_000019.9:g.3958011_3958015dup
GRCh37.p13 chr 19	NC_000019.9:g.3958010_3958015dup

Gene: DAPK3, death associated protein kinase 3 (minus strand) : 500B Downstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
DAPK3 transcript variant 1	NM_001348.3:c.	N/A	Downstream Transcript Variant
DAPK3 transcript variant 2	NM_001375658.1:c.	N/A	Downstream Transcript 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)₁₂	del(A)₁₁	del(A)₁₀	del(A)₉	del(A)₈	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆
GRCh38.p14 chr 19	NC_000019.10:g.3957996_3958017=	NC_000019.10:g.3958006_3958017del	NC_000019.10:g.3958007_3958017del	NC_000019.10:g.3958008_3958017del	NC_000019.10:g.3958009_3958017del	NC_000019.10:g.3958010_3958017del	NC_000019.10:g.3958011_3958017del	NC_000019.10:g.3958012_3958017del	NC_000019.10:g.3958013_3958017del	NC_000019.10:g.3958014_3958017del	NC_000019.10:g.3958015_3958017del	NC_000019.10:g.3958016_3958017del	NC_000019.10:g.3958017del	NC_000019.10:g.3958017dup	NC_000019.10:g.3958016_3958017dup	NC_000019.10:g.3958015_3958017dup	NC_000019.10:g.3958014_3958017dup	NC_000019.10:g.3958013_3958017dup	NC_000019.10:g.3958012_3958017dup
GRCh37.p13 chr 19	NC_000019.9:g.3957994_3958015=	NC_000019.9:g.3958004_3958015del	NC_000019.9:g.3958005_3958015del	NC_000019.9:g.3958006_3958015del	NC_000019.9:g.3958007_3958015del	NC_000019.9:g.3958008_3958015del	NC_000019.9:g.3958009_3958015del	NC_000019.9:g.3958010_3958015del	NC_000019.9:g.3958011_3958015del	NC_000019.9:g.3958012_3958015del	NC_000019.9:g.3958013_3958015del	NC_000019.9:g.3958014_3958015del	NC_000019.9:g.3958015del	NC_000019.9:g.3958015dup	NC_000019.9:g.3958014_3958015dup	NC_000019.9:g.3958013_3958015dup	NC_000019.9:g.3958012_3958015dup	NC_000019.9:g.3958011_3958015dup	NC_000019.9:g.3958010_3958015dup

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#.

43 SubSNP, 27 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41036357	Mar 13, 2006 (126)
2	HUMANGENOME_JCVI	ss95719883	Dec 05, 2013 (138)
3	PJP	ss294951667	May 09, 2011 (138)
4	SSMP	ss664442588	Apr 01, 2015 (144)
5	SWEGEN	ss3016997762	Nov 08, 2017 (151)
6	MCHAISSO	ss3063905145	Nov 08, 2017 (151)
7	EVA_DECODE	ss3702229267	Jul 13, 2019 (153)
8	EVA_DECODE	ss3702229268	Jul 13, 2019 (153)
9	EVA_DECODE	ss3702229269	Jul 13, 2019 (153)
10	EVA_DECODE	ss3702229270	Jul 13, 2019 (153)
11	EVA_DECODE	ss3702229271	Jul 13, 2019 (153)
12	EVA	ss3835321270	Apr 27, 2020 (154)
13	GNOMAD	ss4326722326	Apr 26, 2021 (155)
14	GNOMAD	ss4326722327	Apr 26, 2021 (155)
15	GNOMAD	ss4326722328	Apr 26, 2021 (155)
16	GNOMAD	ss4326722329	Apr 26, 2021 (155)
17	GNOMAD	ss4326722330	Apr 26, 2021 (155)
18	GNOMAD	ss4326722331	Apr 26, 2021 (155)
19	GNOMAD	ss4326722332	Apr 26, 2021 (155)
20	GNOMAD	ss4326722333	Apr 26, 2021 (155)
21	GNOMAD	ss4326722334	Apr 26, 2021 (155)
22	GNOMAD	ss4326722335	Apr 26, 2021 (155)
23	GNOMAD	ss4326722336	Apr 26, 2021 (155)
24	GNOMAD	ss4326722337	Apr 26, 2021 (155)
25	GNOMAD	ss4326722338	Apr 26, 2021 (155)
26	GNOMAD	ss4326722339	Apr 26, 2021 (155)
27	GNOMAD	ss4326722340	Apr 26, 2021 (155)
28	GNOMAD	ss4326722341	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5226464082	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5226464083	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5226464084	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5226464085	Apr 26, 2021 (155)
33	1000G_HIGH_COVERAGE	ss5306290691	Oct 16, 2022 (156)
34	1000G_HIGH_COVERAGE	ss5306290692	Oct 16, 2022 (156)
35	1000G_HIGH_COVERAGE	ss5306290693	Oct 16, 2022 (156)
36	HUGCELL_USP	ss5498949004	Oct 16, 2022 (156)
37	HUGCELL_USP	ss5498949005	Oct 16, 2022 (156)
38	HUGCELL_USP	ss5498949006	Oct 16, 2022 (156)
39	TOMMO_GENOMICS	ss5784647270	Oct 16, 2022 (156)
40	TOMMO_GENOMICS	ss5784647271	Oct 16, 2022 (156)
41	TOMMO_GENOMICS	ss5784647272	Oct 16, 2022 (156)
42	TOMMO_GENOMICS	ss5784647274	Oct 16, 2022 (156)
43	TOMMO_GENOMICS	ss5784647275	Oct 16, 2022 (156)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532522195 (NC_000019.10:3957995::A 40140/56800) Row 532522196 (NC_000019.10:3957995::AA 1840/55268) Row 532522197 (NC_000019.10:3957995::AAA 1592/55754)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532522195 (NC_000019.10:3957995::A 40140/56800) Row 532522196 (NC_000019.10:3957995::AA 1840/55268) Row 532522197 (NC_000019.10:3957995::AAA 1592/55754)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532522195 (NC_000019.10:3957995::A 40140/56800) Row 532522196 (NC_000019.10:3957995::AA 1840/55268) Row 532522197 (NC_000019.10:3957995::AAA 1592/55754)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532522195 (NC_000019.10:3957995::A 40140/56800) Row 532522196 (NC_000019.10:3957995::AA 1840/55268) Row 532522197 (NC_000019.10:3957995::AAA 1592/55754)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532522195 (NC_000019.10:3957995::A 40140/56800) Row 532522196 (NC_000019.10:3957995::AA 1840/55268) Row 532522197 (NC_000019.10:3957995::AAA 1592/55754)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532522195 (NC_000019.10:3957995::A 40140/56800) Row 532522196 (NC_000019.10:3957995::AA 1840/55268) Row 532522197 (NC_000019.10:3957995::AAA 1592/55754)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532522195 (NC_000019.10:3957995::A 40140/56800) Row 532522196 (NC_000019.10:3957995::AA 1840/55268) Row 532522197 (NC_000019.10:3957995::AAA 1592/55754)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532522195 (NC_000019.10:3957995::A 40140/56800) Row 532522196 (NC_000019.10:3957995::AA 1840/55268) Row 532522197 (NC_000019.10:3957995::AAA 1592/55754)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532522195 (NC_000019.10:3957995::A 40140/56800) Row 532522196 (NC_000019.10:3957995::AA 1840/55268) Row 532522197 (NC_000019.10:3957995::AAA 1592/55754)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532522195 (NC_000019.10:3957995::A 40140/56800) Row 532522196 (NC_000019.10:3957995::AA 1840/55268) Row 532522197 (NC_000019.10:3957995::AAA 1592/55754)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532522195 (NC_000019.10:3957995::A 40140/56800) Row 532522196 (NC_000019.10:3957995::AA 1840/55268) Row 532522197 (NC_000019.10:3957995::AAA 1592/55754)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532522195 (NC_000019.10:3957995::A 40140/56800) Row 532522196 (NC_000019.10:3957995::AA 1840/55268) Row 532522197 (NC_000019.10:3957995::AAA 1592/55754)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532522195 (NC_000019.10:3957995::A 40140/56800) Row 532522196 (NC_000019.10:3957995::AA 1840/55268) Row 532522197 (NC_000019.10:3957995::AAA 1592/55754)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532522195 (NC_000019.10:3957995::A 40140/56800) Row 532522196 (NC_000019.10:3957995::AA 1840/55268) Row 532522197 (NC_000019.10:3957995::AAA 1592/55754)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532522195 (NC_000019.10:3957995::A 40140/56800) Row 532522196 (NC_000019.10:3957995::AA 1840/55268) Row 532522197 (NC_000019.10:3957995::AAA 1592/55754)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532522195 (NC_000019.10:3957995::A 40140/56800) Row 532522196 (NC_000019.10:3957995::AA 1840/55268) Row 532522197 (NC_000019.10:3957995::AAA 1592/55754)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532522195 (NC_000019.10:3957995::A 40140/56800) Row 532522196 (NC_000019.10:3957995::AA 1840/55268) Row 532522197 (NC_000019.10:3957995::AAA 1592/55754)...	-	Apr 26, 2021 (155)
61	8.3KJPN Submission ignored due to conflicting rows: Row 84433389 (NC_000019.9:3957993::A 8644/14934) Row 84433390 (NC_000019.9:3957993::AA 719/14934) Row 84433391 (NC_000019.9:3957993::AAA 66/14934)...	-	Apr 26, 2021 (155)
62	8.3KJPN Submission ignored due to conflicting rows: Row 84433389 (NC_000019.9:3957993::A 8644/14934) Row 84433390 (NC_000019.9:3957993::AA 719/14934) Row 84433391 (NC_000019.9:3957993::AAA 66/14934)...	-	Apr 26, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 84433389 (NC_000019.9:3957993::A 8644/14934) Row 84433390 (NC_000019.9:3957993::AA 719/14934) Row 84433391 (NC_000019.9:3957993::AAA 66/14934)...	-	Apr 26, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 84433389 (NC_000019.9:3957993::A 8644/14934) Row 84433390 (NC_000019.9:3957993::AA 719/14934) Row 84433391 (NC_000019.9:3957993::AAA 66/14934)...	-	Apr 26, 2021 (155)
65	14KJPN Submission ignored due to conflicting rows: Row 118484374 (NC_000019.10:3957995::A 12119/20412) Row 118484375 (NC_000019.10:3957995::AA 936/20412) Row 118484376 (NC_000019.10:3957995::AAA 108/20412)...	-	Oct 16, 2022 (156)
66	14KJPN Submission ignored due to conflicting rows: Row 118484374 (NC_000019.10:3957995::A 12119/20412) Row 118484375 (NC_000019.10:3957995::AA 936/20412) Row 118484376 (NC_000019.10:3957995::AAA 108/20412)...	-	Oct 16, 2022 (156)
67	14KJPN Submission ignored due to conflicting rows: Row 118484374 (NC_000019.10:3957995::A 12119/20412) Row 118484375 (NC_000019.10:3957995::AA 936/20412) Row 118484376 (NC_000019.10:3957995::AAA 108/20412)...	-	Oct 16, 2022 (156)
68	14KJPN Submission ignored due to conflicting rows: Row 118484374 (NC_000019.10:3957995::A 12119/20412) Row 118484375 (NC_000019.10:3957995::AA 936/20412) Row 118484376 (NC_000019.10:3957995::AAA 108/20412)...	-	Oct 16, 2022 (156)
69	14KJPN Submission ignored due to conflicting rows: Row 118484374 (NC_000019.10:3957995::A 12119/20412) Row 118484375 (NC_000019.10:3957995::AA 936/20412) Row 118484376 (NC_000019.10:3957995::AAA 108/20412)...	-	Oct 16, 2022 (156)
70	ALFA	NC_000019.10 - 3957996	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)
rs71166946	May 15, 2013 (138)
rs72032354	May 11, 2012 (137)
rs143203126	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4326722341	NC_000019.10:3957995:AAAAAAAAAAAA:	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
9369275771	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4326722340	NC_000019.10:3957995:AAAAAAAAAAA:	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
9369275771	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss3702229271, ss4326722339	NC_000019.10:3957995:AAAAAAAAAA:	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
9369275771	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4326722338	NC_000019.10:3957995:AAAAAAAAA:	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
9369275771	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4326722337	NC_000019.10:3957995:AAAAAAAA:	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
9369275771	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4326722336	NC_000019.10:3957995:AAAAAAA:	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
9369275771	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss5226464085	NC_000019.9:3957993:AAAAAA:	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4326722335, ss5784647275	NC_000019.10:3957995:AAAAAA:	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
9369275771	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4326722334	NC_000019.10:3957995:AAAAA:	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
9369275771	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4326722333	NC_000019.10:3957995:AAAA:	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
9369275771	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
9369275771	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4326722332	NC_000019.10:3957995:AA:	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
9369275771	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3702229270	NC_000019.10:3958003:AA:	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3016997762	NC_000019.9:3957993:A:	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss5498949006	NC_000019.10:3957995:A:	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
9369275771	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3702229269	NC_000019.10:3958004:A:	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss294951667	NC_000019.8:3908994::A	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5226464082	NC_000019.9:3957993::A	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3063905145, ss4326722326, ss5498949004, ss5784647270	NC_000019.10:3957995::A	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
9369275771	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3702229268	NC_000019.10:3958005::A	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss41036357	NT_011255.14:3897993::A	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss95719883	NT_011255.14:3898015::A	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3835321270, ss5226464083	NC_000019.9:3957993::AA	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4326722327, ss5306290692, ss5498949005, ss5784647271	NC_000019.10:3957995::AA	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
9369275771	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3702229267	NC_000019.10:3958005::AA	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss664442588, ss5226464084	NC_000019.9:3957993::AAA	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4326722328, ss5306290691, ss5784647272	NC_000019.10:3957995::AAA	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
9369275771	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4326722329, ss5306290693	NC_000019.10:3957995::AAAA	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
9369275771	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4326722330, ss5784647274	NC_000019.10:3957995::AAAAA	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
9369275771	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4326722331	NC_000019.10:3957995::AAAAAA	NC_000019.10:3957995:AAAAAAAAAAAAA… NC_000019.10:3957995:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs34130331

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

rs34130331