Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121918456
rs121918456
0.720 GeneticVariation BEFREE In the present series of patients from one family, all patients carry the same recurrent mutation Y279C in the PTPN11 gene, exhibiting different phenotypes and a variable expression of multiple lentigines. 24401936

2014

dbSNP: rs121918456
rs121918456
0.720 GeneticVariation BEFREE We hypothesise that some PTPN11 mutations are associated with the typical Noonan syndrome phenotype and that other mutations, such as the Y279C mutation reported here, are associated with both the Noonan syndrome phenotype and with skin pigmentation anomalies, such as multiple lentigines or café au lait spots. 12161596

2002

dbSNP: rs121918456
rs121918456
G 0.720 CausalMutation CLINVAR

dbSNP: rs121918457
rs121918457
T 0.700 CausalMutation CLINVAR

dbSNP: rs121918470
rs121918470
G 0.700 CausalMutation CLINVAR

dbSNP: rs137852814
rs137852814
C 0.700 CausalMutation CLINVAR

dbSNP: rs397507509
rs397507509
C 0.700 CausalMutation CLINVAR

dbSNP: rs397507520
rs397507520
C 0.700 CausalMutation CLINVAR

dbSNP: rs397507539
rs397507539
G 0.700 CausalMutation CLINVAR

dbSNP: rs397507540
rs397507540
T 0.700 CausalMutation CLINVAR

dbSNP: rs397507547
rs397507547
G 0.700 CausalMutation CLINVAR

dbSNP: rs397507548
rs397507548
0.010 GeneticVariation BEFREE We report on a 26-year-old female with features of Noonan syndrome-Multiple Lentigines and a heterozygous mutation: c.1517A > C-p.Gln506Pro in the PTPN11 gene. 22528600

2012

dbSNP: rs397509345
rs397509345
0.010 GeneticVariation BEFREE We report on a 26-year-old female with features of Noonan syndrome-Multiple Lentigines and a heterozygous mutation: c.1517A > C-p.Gln506Pro in the PTPN11 gene. 22528600

2012

dbSNP: rs397507549
rs397507549
0.010 GeneticVariation BEFREE We describe the "LEOPARD syndrome (LS) phenotype" associated with the Gln510Glu mutation of the PTPN11 gene in two patients presenting with rapidly progressive severe biventricular obstructive hypertrophic cardiomyopathy and structural abnormalities of the mitral valve, facial anomalies, café-au-lait spots and multiple lentigines. 16733669

2006