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

C/G/T|Ancestral: C|Ambiguity code: B|MAF: 0.11 (T)

This variant maps to 7 genomic locations; None selected

Evidence status


Archive dbSNP rs114612789, rs117549896

HGVS name


Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 1 regulatory feature and has 3691 sample genotypes.

Variant displays