Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.41 (C)
Location

Chromosome 7:128594725 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR068449

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs10373278, rs56657495

HGVS name

7:g.128594725C>T

This variation has assays on 5 chips - click the plus to show

Variation displays