Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W | MAF: < 0.01 (T)
Location

Chromosome 9:124450082 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

9:g.124450082A>T

About this variant

This variant overlaps 2 transcripts and has 2504 sample genotypes.

Variant displays