This variant maps to 2 locations

Select a location:
Original source

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

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.37 (A)
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs643029

HGVS name

None

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5

About this variant

This variant overlaps 1 regulatory feature and has 2508 sample genotypes.

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