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|MAF: 0.05 (A)

This variant maps to 8 genomic locations; None selected

Evidence status

Clinical significance


This variant has 7 synonyms - Show

HGVS name


Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant has 2881 sample genotypes, is associated with 8 phenotypes and is mentioned in 1 citation.

Variant displays