Original source

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

Alleles
T/G|Ancestral: T|Ambiguity code: K|MAF: < 0.01 (G)
Location

Chromosome 9:99103602 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

9:g.99103602T>G

About this variant

This variant overlaps 6 transcripts and has 2593 sample genotypes.

Variant displays