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
G/T | Ambiguity code: K | MAF: < 0.01 (T)
Location

This variation maps to 3 genomic locations; None selected

Evidence status

HGVS name

None

Variation displays