Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome 17:32581278 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

17:g.32581278A>C

This variation has assays on 4 chips - click the plus to show

Variation displays