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
C/T|Ambiguity code: Y
Location

This variant maps to 3 genomic locations; None selected

Evidence status

HGVS name

None

About this variant

This variant overlaps 1 regulatory feature.

Variant displays