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
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.46 (C)
Location

This variation maps to 3 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs61157165

HGVS name

None

Variation displays