Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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
 
Upstream gene variant
Evidence status

HGVS name

22:g.19151855C>G

Genotyping chips

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

About this variant

This variant overlaps 1 transcript and has 3692 sample genotypes.

Variant displays