This variation maps to 2 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
Location

This variation maps to 2 genomic locations; None selected

Synonyms

Archive dbSNP rs3191334

HGVS name

None

Variation displays