This variation maps to 2 locations

Select a location:
Original source

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

Alleles
G/C | Ancestral: C | Ambiguity code: S
Location

This variation maps to 2 genomic locations; None selected

Evidence status

HGVS name

None

About this variant

This variant overlaps 1 transcript and has 6 individual genotypes.

Variation displays