Original source

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

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

This variant has assays on 7 chips - click the plus to 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