This variant maps to 2 locations

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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|MAF: 0.44 (A)
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

This variant has 6 synonyms - Show

HGVS name

None

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 1 regulatory feature, has 3986 sample genotypes, is associated with 2 phenotypes and is mentioned in 2 citations.

Variant displays