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: 0.39 (C)
Location

This variation maps to 2 genomic locations; None selected

Evidence status

Synonyms
HGVS name

None

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_ExomeChip

About this variant

This variant has 2511 individual genotypes.

Variation displays