Original source

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

Alleles
G/A/C|Ancestral: G|Ambiguity code: V
Location

Chromosome 19:33411697 (forward strand)|View in location tab

Co-located variants

COSMIC COSM88492 ; HGMD-PUBLIC CM060426

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 4576

HGVS names

This variant has 28 HGVS names - Show

About this variant

This variant overlaps 16 transcripts and is associated with 2 phenotypes.

Variant displays