Original source

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

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

Chromosome 11:18392471 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

11:g.18392471G>A

About this variant

This variant overlaps 22 transcripts and has 32 sample genotypes.

Variant displays