OCLN, occludin, 100506658

N. diseases: 195; N. variants: 8
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs749237456
rs749237456
Entrez Id: 100506658
Gene Symbol: OCLN
OCLN
CUI: C4552078
Disease:
PSEUDO-TORCH SYNDROME 1
TA 0.700 CausalMutation CLINVAR