Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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
Evidence status

Synonyms
HGVS name

9:g.22134095T>C

This variation has assays on 7 chips - click the plus to show

About this variant

This variant has 3957 individual genotypes, is associated with 7 phenotypes and is mentioned in 191 citations.

Variation displays