Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.44 (C)
Location

Chromosome 17:32686006 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs56522587, rs59584284

HGVS name

17:g.32686006T>C

This variation has assays on 10 chips - click the plus to show

Variation displays