This variant has been flagged

None of the variant alleles match the reference allele

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
A/T|Ambiguity code: W|MAF: 0.38 (T)
Location

This variant maps to 8 genomic locations; None selected

Evidence status

Synonyms
HGVS name

None

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant has 2691 sample genotypes.

Variant displays