Original source

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

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

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


with HGMD-PUBLIC CR111177

Most severe consequence
Downstream gene variant
Evidence status

HGVS name


This variant has assays on 5 chips - click the plus to 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 156 citations.

Variant displays