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: T | Ambiguity code: Y | MAF: 0.41 (C)
Location

This variation maps to 2 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs3824859

HGVS name

None

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni1-Quad

About this variant

This variant has 2505 individual genotypes and is mentioned in 41 citations.

Variation displays