This variant maps to 2 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.40 (C)
Location

This variant maps to 2 genomic locations; None selected

Evidence status

HGVS name

None

About this variant

This variant has 2508 sample genotypes.

Variant displays