SSUH2, ssu-2 homolog, 51066

N. diseases: 7; N. variants: 35
Disease: LONG QT SYNDROME 9 (disorder) ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs72546668
rs72546668
Entrez Id: 859;51066
Gene Symbol: CAV3;SSUH2
CAV3;SSUH2
CUI: C2678485
Disease:
LONG QT SYNDROME 9 (disorder) 		T 0.800 CausalMutation CLINVAR
dbSNP: rs72546668
rs72546668
Entrez Id: 859;51066
Gene Symbol: CAV3;SSUH2
CAV3;SSUH2
CUI: C2678485
Disease:
LONG QT SYNDROME 9 (disorder) 		0.800 GeneticVariation UNIPROT