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 | MAF: 0.02 (A)
Location

This variation maps to 2 genomic locations; None selected

Evidence status

Clinical significance

This variation has 5 synonyms - click the plus to show

HGVS name

None

This variation has assays on 4 chips - click the plus to show

About this variant

This variant has 2775 individual genotypes, is associated with 4 phenotypes and is mentioned in 12 citations.

Variation displays