Original source

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

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

Chromosome 11:18264340 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

11:g.18264340T>G

About this variant

This variant overlaps 5 transcripts and has 2504 sample genotypes.

Variant displays