This variation maps to 2 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/A | Ancestral: T | Ambiguity code: W
Location

This variation maps to 2 genomic locations; None selected

Evidence status

Clinical significance

HGVS name

None

About this variant

This variant is associated with 3 phenotypes.

Variation displays