Original source

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

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

Chromosome 11:32392032 (forward strand)|View in location tab

Co-located variants

COSMIC COSM4781824, COSM3397637, COSM21397 ; HGMD-PUBLIC CM971596

Most severe consequence
Stop gained
Evidence status

Clinical significance


LSDB 14632, 18533

HGVS names

This variant has 19 HGVS names - Show

About this variant

This variant overlaps 11 transcripts, 1 regulatory feature and is associated with 4 phenotypes.

Variant displays