Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs141138948
rs141138948
EXOSC3
CUI: C0027765
Disease: nervous system disorder
nervous system disorder 		0.010 GeneticVariation BEFREE Homozygosity for the EXOSC3 variant c.395A > C, p.(Asp132Ala) is proposed to lead to a rather mild phenotype compared to compound-heterozygous EXOSC3-pathogenic-variants carriers with lethal neurological disease in very early childhood. 30986545

2020