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/C/T|Ancestral: A|Ambiguity code: H|MAF: 0.37 (C)
Location

This variant maps to 8 genomic locations; None selected

Evidence status

Synonyms
HGVS name

None

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant has 3695 sample genotypes.

Variant displays