Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.01 (A)
Location

Chromosome 11:18393617 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

11:g.18393617G>A

About this variant

This variant overlaps 21 transcripts and has 2504 sample genotypes.

Variant displays