Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/A|Ancestral: A|Ambiguity code: R|MAF: 0.21 (A)
Location

Chromosome 17:76140855 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs3760134

HGVS names

This variant has 4 HGVS names - Hide

17:g.76140855G>A
ENST00000585542.1:n.100+175G>A
ENST00000590137.1:n.125+175G>A
ENST00000322957.6:c.-170+259C>T

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 9 transcripts, 1 regulatory feature, has 2508 sample genotypes and is mentioned in 1 citation.

Variant displays