This variation maps to 5 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
T/A/C | Ancestral: T | Ambiguity code: H | MAF: 0.47 (A)
Location

This variation maps to 5 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs9274566, rs116848421

HGVS name

None

Variation displays