This variation maps to 3 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 | Ambiguity code: Y
Location

This variation maps to 3 genomic locations; None selected

Evidence status

HGVS name

None

About this variant

This variant has 3 individual genotypes.

Variation displays