This variation maps to 7 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

This variation maps to 7 genomic locations; None selected

Evidence status


Archive dbSNP rs59204384, rs113380831

HGVS name


Genotyping chips

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

About this variant

This variant has 2283 individual genotypes and is mentioned in 2 citations.

Variation displays