SSUH2, ssu-2 homolog, 51066

N. diseases: 7; N. variants: 35
Disease: LONG QT SYNDROME 2/9, DIGENIC ×
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: C3279093
Disease:
LONG QT SYNDROME 2/9, DIGENIC 		T 0.700 CausalMutation CLINVAR