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
A/G|Ancestral: A|Ambiguity code: R|MAF: < 0.01 (G)
Location

This variant maps to 8 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

This variant has 3 synonyms - Show

HGVS name

None

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant has 2542 sample genotypes and is associated with 8 phenotypes.

Variant displays