Original source

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

Alleles
G/C|Ancestral: C|Ambiguity code: S|MAF: 0.42 (C)
Location

Chromosome 9:22125504 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms
HGVS name

9:g.22125504G>C

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 10 transcripts, has 4039 sample genotypes, is associated with 8 phenotypes and is mentioned in 185 citations.

Variant displays