SSUH2, ssu-2 homolog, 51066

N. diseases: 7; N. variants: 35
Disease: Sudden infant death syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909281
rs121909281
Entrez Id: 859;51066
Gene Symbol: CAV3;SSUH2
CAV3;SSUH2
CUI: C0038644
Disease:
Sudden infant death syndrome 		0.700 GeneticVariation UNIPROT Novel mechanism for sudden infant death syndrome: persistent late sodium current secondary to mutations in caveolin-3. 17275750 2007