This variant maps to 2 locations

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Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.29 (A)
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs59331249

HGVS name

None

This variant has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 1 regulatory feature and has 2902 sample genotypes.

Variant displays