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/C | Ancestral: C | Ambiguity code: Y | MAF: 0.35 (C)
Location

This variation maps to 2 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs34912150, rs59821819

HGVS name

None

This variation has assays on 13 chips - click the plus to show

About this variant

This variant has 4279 individual genotypes, is associated with 3 phenotypes and is mentioned in 17 citations.

Variation displays