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
Location

This variant maps to 6 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs115353040, rs117224193

HGVS name

None

Variant displays