Disease: NOONAN SYNDROME 9 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs373233749
rs373233749
Entrez Id: 6655
Gene Symbol: SOS2
SOS2
CUI: C4225282
Disease:
NOONAN SYNDROME 9 		0.700 GeneticVariation UNIPROT Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome. 25795793 2015