This variation maps to 7 locations

Select a location:
Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W | MAF: 0.20 (T)
Location

This variation maps to 7 genomic locations; None selected

Evidence status

Synonyms
HGVS name

None

Variation displays