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
G/A|Ancestral: G|Ambiguity code: R
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

LSDB 13849

HGVS name

None

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant is associated with 4 phenotypes and is mentioned in 1 citation.

Variant displays