Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.49 (C)
Location

Chromosome 22:19139368 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

22:g.19139368C>G

Genotyping chips

This variation has assays on: Affy GenomeWideSNP_6.0, Illumina_HumanOmni2.5, Illumina_HumanOmni5

Variation displays