Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.27 (T)
Location

Chromosome 9:114806766 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

9:g.114806766T>C

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 1 transcript, 1 regulatory feature, has 3766 sample genotypes, is associated with 1 phenotype and is mentioned in 19 citations.

Variant displays