Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.18 (C)
Location

Chromosome 9:22134095 (forward strand)|View in location tab

Most severe consequence
 
Intergenic variant
Evidence status

Synonyms
HGVS name

9:g.22134095T>C

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant has 3957 sample genotypes, is associated with 8 phenotypes and is mentioned in 198 citations.

Variant displays