rs397507545, PTPN11

N. diseases: 20
Disease: Gastroesophageal reflux disease ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Gastroesophageal reflux disease
CUI: C0017168
Disease: Gastroesophageal reflux disease
0.700 CausalMutation CLINVAR Diversity and functional consequences of germline and somatic PTPN11 mutations in human disease. 16358218 2006
Gastroesophageal reflux disease
CUI: C0017168
Disease: Gastroesophageal reflux disease
0.700 CausalMutation CLINVAR The mutational spectrum of PTPN11 in juvenile myelomonocytic leukemia and Noonan syndrome/myeloproliferative disease. 15928039 2005
Gastroesophageal reflux disease
CUI: C0017168
Disease: Gastroesophageal reflux disease
0.700 CausalMutation CLINVAR Genotype-phenotype correlations in Noonan syndrome. 15001945 2004
Gastroesophageal reflux disease
CUI: C0017168
Disease: Gastroesophageal reflux disease
0.700 CausalMutation CLINVAR Somatic mutations in PTPN11 in juvenile myelomonocytic leukemia, myelodysplastic syndromes and acute myeloid leukemia. 12717436 2003