This variation maps to 8 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.08 (C)
Location

This variation maps to 8 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs115061932, rs118100802

HGVS name

None

About this variant

This variant has 1097 individual genotypes.

Variation displays