Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.29 (A)
Location

Chromosome 7:128933913 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR084006

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs61010776

HGVS name

7:g.128933913G>A

Genotyping chips

This variant has assays on 13 chips - Show

About this variant

This variant overlaps 11 transcripts, 1 regulatory feature, has 3963 sample genotypes, is associated with 5 phenotypes and is mentioned in 41 citations.

Variant displays