Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.30 (A)
Location

Chromosome 7:128573967 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR084006

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61010776

HGVS name

7:g.128573967G>A

This variation has assays on 11 chips - click the plus to show

Variation displays