Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R
Location

Chromosome 9:99103541 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

9:g.99103541A>G

About this variant

This variant overlaps 6 transcripts and has 89 sample genotypes.

Variant displays