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

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

This variant maps to 8 genomic locations; None selected

Evidence status

Synonyms

This variant has 2 synonyms - Show

HGVS name

None

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 1 regulatory feature and is mentioned in 2 citations.

Variant displays