Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894366
rs104894366
KRAS
C 0.700 CausalMutation CLINVAR Structure-energy-based predictions and network modelling of RASopathy and cancer missense mutations. 24803665

2014
dbSNP: rs104894366
rs104894366
KRAS
C 0.700 CausalMutation CLINVAR Germline KRAS mutations cause aberrant biochemical and physical properties leading to developmental disorders. 20949621

2011
dbSNP: rs104894366
rs104894366
KRAS
C 0.700 CausalMutation CLINVAR Germline KRAS mutations cause Noonan syndrome. 16474405

2006