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
T/C|Ambiguity code: Y|MAF: 0.27 (T)
Location

This variant maps to 7 genomic locations; None selected

Evidence status

Synonyms
HGVS name

None

Genotyping chips

This variant has assays on 13 chips - Show

About this variant

This variant has 4024 sample genotypes, is associated with 49 phenotypes and is mentioned in 19 citations.

Variant displays