Name: rs34926290
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.

rs34926290

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr16:83806003-83806026 (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)₁₅ / del(A)₁₄ / del(A)₁₃ / d…
del(A)₁₅ / del(A)₁₄ / del(A)₁₃ / 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 / dup(A)₇ / dup(A)₈ / dup(A)₉ / dup(A)₁₄
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₅=0.0000 (0/1012, ALFA)
del(A)₁₄=0.0000 (0/1012, ALFA)
del(A)₁₃=0.0000 (0/1012, ALFA) (+ 15 more)
del(A)₁₂=0.0000 (0/1012, ALFA)
del(A)₁₁=0.0000 (0/1012, ALFA)
del(A)₁₀=0.0000 (0/1012, ALFA)
del(A)₉=0.0000 (0/1012, ALFA)
del(A)₈=0.0000 (0/1012, ALFA)
del(A)₇=0.0000 (0/1012, ALFA)
del(A)₆=0.0000 (0/1012, ALFA)
del(A)₅=0.0000 (0/1012, ALFA)
del(A)₄=0.0000 (0/1012, ALFA)
delAAA=0.0000 (0/1012, ALFA)
delAA=0.0000 (0/1012, ALFA)
delA=0.0000 (0/1012, ALFA)
dupA=0.0000 (0/1012, ALFA)
dupAA=0.0000 (0/1012, ALFA)
dupAAA=0.0000 (0/1012, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: HSBP1 : 2KB Upstream 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	1012	AAAAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, 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, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	540	AAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, 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, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African	Sub	164	AAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, 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, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	2	AAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, 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, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
African American	Sub	162	AAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, 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, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	46	AAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, 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, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	38	AAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, 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, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	8	AAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, 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, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	16	AAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, 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, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	172	AAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, 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, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	12	AAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, 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, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	62	AAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, 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, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	1012	(A)₂₄=1.0000	del(A)₁₅=0.0000, del(A)₁₄=0.0000, del(A)₁₃=0.0000, 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
Allele Frequency Aggregator	European	Sub	540	(A)₂₄=1.000	del(A)₁₅=0.000, del(A)₁₄=0.000, del(A)₁₃=0.000, 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
Allele Frequency Aggregator	Latin American 2	Sub	172	(A)₂₄=1.000	del(A)₁₅=0.000, del(A)₁₄=0.000, del(A)₁₃=0.000, 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
Allele Frequency Aggregator	African	Sub	164	(A)₂₄=1.000	del(A)₁₅=0.000, del(A)₁₄=0.000, del(A)₁₃=0.000, 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
Allele Frequency Aggregator	Other	Sub	62	(A)₂₄=1.00	del(A)₁₅=0.00, del(A)₁₄=0.00, del(A)₁₃=0.00, 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
Allele Frequency Aggregator	Asian	Sub	46	(A)₂₄=1.00	del(A)₁₅=0.00, del(A)₁₄=0.00, del(A)₁₃=0.00, 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
Allele Frequency Aggregator	Latin American 1	Sub	16	(A)₂₄=1.00	del(A)₁₅=0.00, del(A)₁₄=0.00, del(A)₁₃=0.00, 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
Allele Frequency Aggregator	South Asian	Sub	12	(A)₂₄=1.00	del(A)₁₅=0.00, del(A)₁₄=0.00, del(A)₁₃=0.00, 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

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 16	NC_000016.10:g.83806012_83806026del
GRCh38.p14 chr 16	NC_000016.10:g.83806013_83806026del
GRCh38.p14 chr 16	NC_000016.10:g.83806014_83806026del
GRCh38.p14 chr 16	NC_000016.10:g.83806015_83806026del
GRCh38.p14 chr 16	NC_000016.10:g.83806016_83806026del
GRCh38.p14 chr 16	NC_000016.10:g.83806017_83806026del
GRCh38.p14 chr 16	NC_000016.10:g.83806018_83806026del
GRCh38.p14 chr 16	NC_000016.10:g.83806019_83806026del
GRCh38.p14 chr 16	NC_000016.10:g.83806020_83806026del
GRCh38.p14 chr 16	NC_000016.10:g.83806021_83806026del
GRCh38.p14 chr 16	NC_000016.10:g.83806022_83806026del
GRCh38.p14 chr 16	NC_000016.10:g.83806023_83806026del
GRCh38.p14 chr 16	NC_000016.10:g.83806024_83806026del
GRCh38.p14 chr 16	NC_000016.10:g.83806025_83806026del
GRCh38.p14 chr 16	NC_000016.10:g.83806026del
GRCh38.p14 chr 16	NC_000016.10:g.83806026dup
GRCh38.p14 chr 16	NC_000016.10:g.83806025_83806026dup
GRCh38.p14 chr 16	NC_000016.10:g.83806024_83806026dup
GRCh38.p14 chr 16	NC_000016.10:g.83806023_83806026dup
GRCh38.p14 chr 16	NC_000016.10:g.83806022_83806026dup
GRCh38.p14 chr 16	NC_000016.10:g.83806021_83806026dup
GRCh38.p14 chr 16	NC_000016.10:g.83806020_83806026dup
GRCh38.p14 chr 16	NC_000016.10:g.83806019_83806026dup
GRCh38.p14 chr 16	NC_000016.10:g.83806018_83806026dup
GRCh38.p14 chr 16	NC_000016.10:g.83806013_83806026dup
GRCh37.p13 chr 16	NC_000016.9:g.83839617_83839631del
GRCh37.p13 chr 16	NC_000016.9:g.83839618_83839631del
GRCh37.p13 chr 16	NC_000016.9:g.83839619_83839631del
GRCh37.p13 chr 16	NC_000016.9:g.83839620_83839631del
GRCh37.p13 chr 16	NC_000016.9:g.83839621_83839631del
GRCh37.p13 chr 16	NC_000016.9:g.83839622_83839631del
GRCh37.p13 chr 16	NC_000016.9:g.83839623_83839631del
GRCh37.p13 chr 16	NC_000016.9:g.83839624_83839631del
GRCh37.p13 chr 16	NC_000016.9:g.83839625_83839631del
GRCh37.p13 chr 16	NC_000016.9:g.83839626_83839631del
GRCh37.p13 chr 16	NC_000016.9:g.83839627_83839631del
GRCh37.p13 chr 16	NC_000016.9:g.83839628_83839631del
GRCh37.p13 chr 16	NC_000016.9:g.83839629_83839631del
GRCh37.p13 chr 16	NC_000016.9:g.83839630_83839631del
GRCh37.p13 chr 16	NC_000016.9:g.83839631del
GRCh37.p13 chr 16	NC_000016.9:g.83839631dup
GRCh37.p13 chr 16	NC_000016.9:g.83839630_83839631dup
GRCh37.p13 chr 16	NC_000016.9:g.83839629_83839631dup
GRCh37.p13 chr 16	NC_000016.9:g.83839628_83839631dup
GRCh37.p13 chr 16	NC_000016.9:g.83839627_83839631dup
GRCh37.p13 chr 16	NC_000016.9:g.83839626_83839631dup
GRCh37.p13 chr 16	NC_000016.9:g.83839625_83839631dup
GRCh37.p13 chr 16	NC_000016.9:g.83839624_83839631dup
GRCh37.p13 chr 16	NC_000016.9:g.83839623_83839631dup
GRCh37.p13 chr 16	NC_000016.9:g.83839618_83839631dup

Gene: HSBP1, heat shock factor binding protein 1 (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
HSBP1 transcript	NM_001537.4:c.	N/A	Upstream 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)₂₄=	del(A)₁₅	del(A)₁₄	del(A)₁₃	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	dup(A)₇	dup(A)₈	dup(A)₉	dup(A)₁₄
GRCh38.p14 chr 16	NC_000016.10:g.83806003_83806026=	NC_000016.10:g.83806012_83806026del	NC_000016.10:g.83806013_83806026del	NC_000016.10:g.83806014_83806026del	NC_000016.10:g.83806015_83806026del	NC_000016.10:g.83806016_83806026del	NC_000016.10:g.83806017_83806026del	NC_000016.10:g.83806018_83806026del	NC_000016.10:g.83806019_83806026del	NC_000016.10:g.83806020_83806026del	NC_000016.10:g.83806021_83806026del	NC_000016.10:g.83806022_83806026del	NC_000016.10:g.83806023_83806026del	NC_000016.10:g.83806024_83806026del	NC_000016.10:g.83806025_83806026del	NC_000016.10:g.83806026del	NC_000016.10:g.83806026dup	NC_000016.10:g.83806025_83806026dup	NC_000016.10:g.83806024_83806026dup	NC_000016.10:g.83806023_83806026dup	NC_000016.10:g.83806022_83806026dup	NC_000016.10:g.83806021_83806026dup	NC_000016.10:g.83806020_83806026dup	NC_000016.10:g.83806019_83806026dup	NC_000016.10:g.83806018_83806026dup	NC_000016.10:g.83806013_83806026dup
GRCh37.p13 chr 16	NC_000016.9:g.83839608_83839631=	NC_000016.9:g.83839617_83839631del	NC_000016.9:g.83839618_83839631del	NC_000016.9:g.83839619_83839631del	NC_000016.9:g.83839620_83839631del	NC_000016.9:g.83839621_83839631del	NC_000016.9:g.83839622_83839631del	NC_000016.9:g.83839623_83839631del	NC_000016.9:g.83839624_83839631del	NC_000016.9:g.83839625_83839631del	NC_000016.9:g.83839626_83839631del	NC_000016.9:g.83839627_83839631del	NC_000016.9:g.83839628_83839631del	NC_000016.9:g.83839629_83839631del	NC_000016.9:g.83839630_83839631del	NC_000016.9:g.83839631del	NC_000016.9:g.83839631dup	NC_000016.9:g.83839630_83839631dup	NC_000016.9:g.83839629_83839631dup	NC_000016.9:g.83839628_83839631dup	NC_000016.9:g.83839627_83839631dup	NC_000016.9:g.83839626_83839631dup	NC_000016.9:g.83839625_83839631dup	NC_000016.9:g.83839624_83839631dup	NC_000016.9:g.83839623_83839631dup	NC_000016.9:g.83839618_83839631dup

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#.

48 SubSNP, 34 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40692366	Mar 14, 2006 (126)
2	HUMANGENOME_JCVI	ss96716419	Feb 13, 2009 (137)
3	SWEGEN	ss3014934103	Nov 08, 2017 (151)
4	EVA	ss3834698063	Apr 27, 2020 (154)
5	GNOMAD	ss4305453543	Apr 26, 2021 (155)
6	GNOMAD	ss4305453544	Apr 26, 2021 (155)
7	GNOMAD	ss4305453545	Apr 26, 2021 (155)
8	GNOMAD	ss4305453546	Apr 26, 2021 (155)
9	GNOMAD	ss4305453547	Apr 26, 2021 (155)
10	GNOMAD	ss4305453548	Apr 26, 2021 (155)
11	GNOMAD	ss4305453549	Apr 26, 2021 (155)
12	GNOMAD	ss4305453550	Apr 26, 2021 (155)
13	GNOMAD	ss4305453551	Apr 26, 2021 (155)
14	GNOMAD	ss4305453552	Apr 26, 2021 (155)
15	GNOMAD	ss4305453553	Apr 26, 2021 (155)
16	GNOMAD	ss4305453554	Apr 26, 2021 (155)
17	GNOMAD	ss4305453555	Apr 26, 2021 (155)
18	GNOMAD	ss4305453556	Apr 26, 2021 (155)
19	GNOMAD	ss4305453557	Apr 26, 2021 (155)
20	GNOMAD	ss4305453558	Apr 26, 2021 (155)
21	GNOMAD	ss4305453559	Apr 26, 2021 (155)
22	GNOMAD	ss4305453560	Apr 26, 2021 (155)
23	GNOMAD	ss4305453561	Apr 26, 2021 (155)
24	GNOMAD	ss4305453562	Apr 26, 2021 (155)
25	GNOMAD	ss4305453563	Apr 26, 2021 (155)
26	GNOMAD	ss4305453564	Apr 26, 2021 (155)
27	GNOMAD	ss4305453565	Apr 26, 2021 (155)
28	GNOMAD	ss4305453566	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5220757199	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5220757200	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5220757201	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5220757202	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5220757203	Apr 26, 2021 (155)
34	1000G_HIGH_COVERAGE	ss5301865712	Oct 17, 2022 (156)
35	1000G_HIGH_COVERAGE	ss5301865713	Oct 17, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5301865714	Oct 17, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5301865715	Oct 17, 2022 (156)
38	1000G_HIGH_COVERAGE	ss5301865716	Oct 17, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5301865717	Oct 17, 2022 (156)
40	HUGCELL_USP	ss5495120330	Oct 17, 2022 (156)
41	HUGCELL_USP	ss5495120331	Oct 17, 2022 (156)
42	HUGCELL_USP	ss5495120332	Oct 17, 2022 (156)
43	HUGCELL_USP	ss5495120333	Oct 17, 2022 (156)
44	SANFORD_IMAGENETICS	ss5659408552	Oct 17, 2022 (156)
45	TOMMO_GENOMICS	ss5776109334	Oct 17, 2022 (156)
46	TOMMO_GENOMICS	ss5776109335	Oct 17, 2022 (156)
47	TOMMO_GENOMICS	ss5776109336	Oct 17, 2022 (156)
48	TOMMO_GENOMICS	ss5776109337	Oct 17, 2022 (156)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497136622 (NC_000016.10:83806002::A 19738/61310) Row 497136623 (NC_000016.10:83806002::AA 4477/61242) Row 497136624 (NC_000016.10:83806002::AAA 245/61274)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497136622 (NC_000016.10:83806002::A 19738/61310) Row 497136623 (NC_000016.10:83806002::AA 4477/61242) Row 497136624 (NC_000016.10:83806002::AAA 245/61274)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497136622 (NC_000016.10:83806002::A 19738/61310) Row 497136623 (NC_000016.10:83806002::AA 4477/61242) Row 497136624 (NC_000016.10:83806002::AAA 245/61274)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497136622 (NC_000016.10:83806002::A 19738/61310) Row 497136623 (NC_000016.10:83806002::AA 4477/61242) Row 497136624 (NC_000016.10:83806002::AAA 245/61274)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497136622 (NC_000016.10:83806002::A 19738/61310) Row 497136623 (NC_000016.10:83806002::AA 4477/61242) Row 497136624 (NC_000016.10:83806002::AAA 245/61274)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497136622 (NC_000016.10:83806002::A 19738/61310) Row 497136623 (NC_000016.10:83806002::AA 4477/61242) Row 497136624 (NC_000016.10:83806002::AAA 245/61274)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497136622 (NC_000016.10:83806002::A 19738/61310) Row 497136623 (NC_000016.10:83806002::AA 4477/61242) Row 497136624 (NC_000016.10:83806002::AAA 245/61274)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497136622 (NC_000016.10:83806002::A 19738/61310) Row 497136623 (NC_000016.10:83806002::AA 4477/61242) Row 497136624 (NC_000016.10:83806002::AAA 245/61274)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497136622 (NC_000016.10:83806002::A 19738/61310) Row 497136623 (NC_000016.10:83806002::AA 4477/61242) Row 497136624 (NC_000016.10:83806002::AAA 245/61274)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497136622 (NC_000016.10:83806002::A 19738/61310) Row 497136623 (NC_000016.10:83806002::AA 4477/61242) Row 497136624 (NC_000016.10:83806002::AAA 245/61274)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497136622 (NC_000016.10:83806002::A 19738/61310) Row 497136623 (NC_000016.10:83806002::AA 4477/61242) Row 497136624 (NC_000016.10:83806002::AAA 245/61274)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497136622 (NC_000016.10:83806002::A 19738/61310) Row 497136623 (NC_000016.10:83806002::AA 4477/61242) Row 497136624 (NC_000016.10:83806002::AAA 245/61274)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497136622 (NC_000016.10:83806002::A 19738/61310) Row 497136623 (NC_000016.10:83806002::AA 4477/61242) Row 497136624 (NC_000016.10:83806002::AAA 245/61274)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497136622 (NC_000016.10:83806002::A 19738/61310) Row 497136623 (NC_000016.10:83806002::AA 4477/61242) Row 497136624 (NC_000016.10:83806002::AAA 245/61274)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497136622 (NC_000016.10:83806002::A 19738/61310) Row 497136623 (NC_000016.10:83806002::AA 4477/61242) Row 497136624 (NC_000016.10:83806002::AAA 245/61274)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497136622 (NC_000016.10:83806002::A 19738/61310) Row 497136623 (NC_000016.10:83806002::AA 4477/61242) Row 497136624 (NC_000016.10:83806002::AAA 245/61274)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497136622 (NC_000016.10:83806002::A 19738/61310) Row 497136623 (NC_000016.10:83806002::AA 4477/61242) Row 497136624 (NC_000016.10:83806002::AAA 245/61274)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497136622 (NC_000016.10:83806002::A 19738/61310) Row 497136623 (NC_000016.10:83806002::AA 4477/61242) Row 497136624 (NC_000016.10:83806002::AAA 245/61274)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497136622 (NC_000016.10:83806002::A 19738/61310) Row 497136623 (NC_000016.10:83806002::AA 4477/61242) Row 497136624 (NC_000016.10:83806002::AAA 245/61274)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497136622 (NC_000016.10:83806002::A 19738/61310) Row 497136623 (NC_000016.10:83806002::AA 4477/61242) Row 497136624 (NC_000016.10:83806002::AAA 245/61274)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497136622 (NC_000016.10:83806002::A 19738/61310) Row 497136623 (NC_000016.10:83806002::AA 4477/61242) Row 497136624 (NC_000016.10:83806002::AAA 245/61274)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497136622 (NC_000016.10:83806002::A 19738/61310) Row 497136623 (NC_000016.10:83806002::AA 4477/61242) Row 497136624 (NC_000016.10:83806002::AAA 245/61274)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497136622 (NC_000016.10:83806002::A 19738/61310) Row 497136623 (NC_000016.10:83806002::AA 4477/61242) Row 497136624 (NC_000016.10:83806002::AAA 245/61274)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497136622 (NC_000016.10:83806002::A 19738/61310) Row 497136623 (NC_000016.10:83806002::AA 4477/61242) Row 497136624 (NC_000016.10:83806002::AAA 245/61274)...	-	Apr 26, 2021 (155)
73	8.3KJPN Submission ignored due to conflicting rows: Row 78726506 (NC_000016.9:83839607::A 846/16662) Row 78726507 (NC_000016.9:83839607:AA: 589/16662) Row 78726508 (NC_000016.9:83839607:A: 2437/16662)...	-	Apr 26, 2021 (155)
74	8.3KJPN Submission ignored due to conflicting rows: Row 78726506 (NC_000016.9:83839607::A 846/16662) Row 78726507 (NC_000016.9:83839607:AA: 589/16662) Row 78726508 (NC_000016.9:83839607:A: 2437/16662)...	-	Apr 26, 2021 (155)
75	8.3KJPN Submission ignored due to conflicting rows: Row 78726506 (NC_000016.9:83839607::A 846/16662) Row 78726507 (NC_000016.9:83839607:AA: 589/16662) Row 78726508 (NC_000016.9:83839607:A: 2437/16662)...	-	Apr 26, 2021 (155)
76	8.3KJPN Submission ignored due to conflicting rows: Row 78726506 (NC_000016.9:83839607::A 846/16662) Row 78726507 (NC_000016.9:83839607:AA: 589/16662) Row 78726508 (NC_000016.9:83839607:A: 2437/16662)...	-	Apr 26, 2021 (155)
77	8.3KJPN Submission ignored due to conflicting rows: Row 78726506 (NC_000016.9:83839607::A 846/16662) Row 78726507 (NC_000016.9:83839607:AA: 589/16662) Row 78726508 (NC_000016.9:83839607:A: 2437/16662)...	-	Apr 26, 2021 (155)
78	14KJPN Submission ignored due to conflicting rows: Row 109946438 (NC_000016.10:83806002:AA: 1201/28036) Row 109946439 (NC_000016.10:83806002::A 1271/28036) Row 109946440 (NC_000016.10:83806002:A: 4841/28036)...	-	Oct 17, 2022 (156)
79	14KJPN Submission ignored due to conflicting rows: Row 109946438 (NC_000016.10:83806002:AA: 1201/28036) Row 109946439 (NC_000016.10:83806002::A 1271/28036) Row 109946440 (NC_000016.10:83806002:A: 4841/28036)...	-	Oct 17, 2022 (156)
80	14KJPN Submission ignored due to conflicting rows: Row 109946438 (NC_000016.10:83806002:AA: 1201/28036) Row 109946439 (NC_000016.10:83806002::A 1271/28036) Row 109946440 (NC_000016.10:83806002:A: 4841/28036)...	-	Oct 17, 2022 (156)
81	14KJPN Submission ignored due to conflicting rows: Row 109946438 (NC_000016.10:83806002:AA: 1201/28036) Row 109946439 (NC_000016.10:83806002::A 1271/28036) Row 109946440 (NC_000016.10:83806002:A: 4841/28036)...	-	Oct 17, 2022 (156)
82	ALFA	NC_000016.10 - 83806003	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)
rs71382880	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4305453566	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAA:	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
734188569	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
ss4305453565	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAA:	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
734188569	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4305453564	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAA:	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
734188569	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4305453563	NC_000016.10:83806002:AAAAAAAAAAAA:	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
734188569	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4305453562	NC_000016.10:83806002:AAAAAAAAAAA:	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
734188569	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss5220757203, ss5659408552	NC_000016.9:83839607:AAAAAAAAAA:	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4305453561	NC_000016.10:83806002:AAAAAAAAAA:	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
734188569	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4305453560	NC_000016.10:83806002:AAAAAAAAA:	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
734188569	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4305453559	NC_000016.10:83806002:AAAAAAAA:	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
734188569	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4305453558	NC_000016.10:83806002:AAAAAAA:	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
734188569	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4305453557	NC_000016.10:83806002:AAAAAA:	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
734188569	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
734188569	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4305453556	NC_000016.10:83806002:AAAA:	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
734188569	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4305453555, ss5301865717	NC_000016.10:83806002:AAA:	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
734188569	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3014934103, ss5220757200	NC_000016.9:83839607:AA:	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4305453554, ss5301865714, ss5495120333, ss5776109334	NC_000016.10:83806002:AA:	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
734188569	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss5220757201	NC_000016.9:83839607:A:	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4305453553, ss5301865715, ss5495120330, ss5776109336	NC_000016.10:83806002:A:	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
734188569	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss40692366	NT_010498.15:37453826:A:	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss96716419	NT_010498.15:37453829:A:	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5220757199	NC_000016.9:83839607::A	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4305453543, ss5301865712, ss5495120331, ss5776109335	NC_000016.10:83806002::A	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
734188569	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3834698063, ss5220757202	NC_000016.9:83839607::AA	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4305453544, ss5301865716, ss5495120332, ss5776109337	NC_000016.10:83806002::AA	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
734188569	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4305453545, ss5301865713	NC_000016.10:83806002::AAA	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
734188569	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4305453546	NC_000016.10:83806002::AAAA	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4305453547	NC_000016.10:83806002::AAAAA	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4305453548	NC_000016.10:83806002::AAAAAA	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4305453549	NC_000016.10:83806002::AAAAAAA	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4305453550	NC_000016.10:83806002::AAAAAAAA	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4305453551	NC_000016.10:83806002::AAAAAAAAA	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4305453552	NC_000016.10:83806002::AAAAAAAAAAA… NC_000016.10:83806002::AAAAAAAAAAAAAA	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3253342931	NC_000016.10:83806002:AAAAA:	NC_000016.10:83806002:AAAAAAAAAAAA… NC_000016.10:83806002:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA

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

No publications for rs34926290

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

rs34926290