Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1563266658
rs1563266658
KRIT1
C 0.700 CausalMutation CLINVAR CCM molecular screening in a diagnosis context: novel unclassified variants leading to abnormal splicing and importance of large deletions. 23595507

2013
dbSNP: rs1563266658
rs1563266658
KRIT1
C 0.700 CausalMutation CLINVAR Clinical, magnetic resonance imaging, and genetic study of 5 Italian families with cerebral cavernous malformation. 17562932

2007