Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs111033632
rs111033632
0.800 GeneticVariation UNIPROT NOTCH2 mutations cause Alagille syndrome, a heterogeneous disorder of the notch signaling pathway. 16773578

2006

dbSNP: rs111033632
rs111033632
T 0.800 CausalMutation CLINVAR

dbSNP: rs1557804111
rs1557804111
A 0.700 GeneticVariation CLINVAR

dbSNP: rs312262798
rs312262798
T 0.700 CausalMutation CLINVAR