Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs727503110
rs727503110
KRAS
CUI: C1860991
Disease: NOONAN SYNDROME 3
NOONAN SYNDROME 3 		0.800 GeneticVariation UNIPROT

dbSNP: rs727503110
rs727503110
KRAS
CUI: C1860991
Disease: NOONAN SYNDROME 3
NOONAN SYNDROME 3 		C 0.800 CausalMutation CLINVAR