Disease: Noonan Syndrome 1 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908595
rs121908595
Entrez Id: 5604
Gene Symbol: MAP2K1
MAP2K1
CUI: C4551602
Disease:
Noonan Syndrome 1 		G 0.700 CausalMutation CLINVAR
dbSNP: rs876657651
rs876657651
Entrez Id: 5604
Gene Symbol: MAP2K1
MAP2K1
CUI: C4551602
Disease:
Noonan Syndrome 1 		G 0.700 GeneticVariation CLINVAR