Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

with HGMD-PUBLIC CR084006

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs61010776

HGVS name

7:g.128933913G>A

This variant has assays on 13 chips - click the plus to 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 40 citations.

Variant displays