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|Ancestral: T|Ambiguity code: Y|MAF: 0.23 (C)
Location

This variant maps to 6 genomic locations; None selected

Evidence status

Synonyms
HGVS name

None

About this variant

This variant has 3042 sample genotypes.

Variant displays