Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.36 (A)
Location

Chromosome 17:38040763 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60658931, rs17305854

HGVS name

17:g.38040763G>A

This variation has assays on 13 chips - click the plus to show

Variation displays