Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W | MAF: 0.16 (A)
Location

Chromosome 10:6122009 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR075253

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs56584268

HGVS name

10:g.6122009T>A

This variation has assays on 8 chips - click the plus to show

Variation displays