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
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.02 (G)
Location

This variation maps to 2 genomic locations; None selected

Evidence status

HGVS name

None

About this variant

This variant has 2504 individual genotypes.

Variation displays