Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397516903
rs397516903
BRAF
CUI: C0028326
Disease: Noonan Syndrome
Noonan Syndrome 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs397516903
rs397516903
BRAF
CUI: C0028326
Disease: Noonan Syndrome
Noonan Syndrome 		C 0.700 GeneticVariation CLINVAR