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

T/A|Ancestral: T|Ambiguity code: W

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance

HGVS name


About this variant

This variant is associated with 4 phenotypes.

Variant displays