This variant maps to 2 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
A/C|Ancestral: A|Ambiguity code: M|MAF: 0.19 (C)
Location

This variant maps to 2 genomic locations; None selected

Evidence status

HGVS name

None

About this variant

This variant overlaps 1 regulatory feature and has 2505 sample genotypes.

Variant displays