Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894366
rs104894366
C 0.800 CausalMutation CLINVAR Structure-energy-based predictions and network modelling of RASopathy and cancer missense mutations. 24803665

2014

dbSNP: rs104894366
rs104894366
C 0.800 CausalMutation CLINVAR Germline KRAS mutations cause aberrant biochemical and physical properties leading to developmental disorders. 20949621

2011

dbSNP: rs104894366
rs104894366
C 0.800 CausalMutation CLINVAR Germline KRAS mutations cause Noonan syndrome. 16474405

2006

dbSNP: rs104894359
rs104894359
G 0.800 CausalMutation CLINVAR

dbSNP: rs387907205
rs387907205
G 0.800 CausalMutation CLINVAR

dbSNP: rs387907206
rs387907206
C 0.800 CausalMutation CLINVAR

dbSNP: rs104894360
rs104894360
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894361
rs104894361
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894362
rs104894362
C 0.700 CausalMutation CLINVAR

dbSNP: rs727503110
rs727503110
C 0.700 CausalMutation CLINVAR

dbSNP: rs730880471
rs730880471
T 0.700 GeneticVariation CLINVAR