Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.41 (G)
Location

Chromosome 9:22124478 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR111177

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

9:g.22124478A>G

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 10 transcripts, 1 regulatory feature, has 2739 sample genotypes, is associated with 1 phenotype and is mentioned in 161 citations.

Variant displays