Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.45 (C)
Location

Chromosome 22:19151855 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

22:g.19151855C>G

Genotyping chips

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

About this variant

This variant overlaps 1 transcript and has 3692 individual genotypes.

Variation displays