This variant has been flagged

None of the variant alleles match the reference allele

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Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

T/G | Ancestral: T | Ambiguity code: K | MAF: 0.28 (G)

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance


This variant has 8 synonyms - Show

HGVS name


Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant has 4036 sample genotypes, is associated with 8 phenotypes and is mentioned in 5 citations.

Variant displays