This variant has been flagged

None of the variant alleles match the reference allele

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Original source

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

C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.45 (T)

This variant maps to 10 genomic locations; None selected

Evidence status


Archive dbSNP rs61151819, rs17699779

HGVS name


Genotyping chips

This variant has assays on 12 chips - Show

About this variant

This variant has 4032 sample genotypes and is mentioned in 2 citations.

Variant displays