This variation maps to 7 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.11 (G)
Location

This variation maps to 7 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs59204384, rs113380831

HGVS name

None

Genotyping chips

This variation has assays on: Affy GeneChip 500K, Affy GenomeWideSNP_6.0, Illumina_HumanOmni5

Variation displays