rs121913496, LRRC56;HRAS

N. diseases: 16
Disease: NOONAN SYNDROME 3 ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
NOONAN SYNDROME 3
CUI: C1860991
Disease: NOONAN SYNDROME 3
0.700 GeneticVariation CLINVAR Differential regulation of rasGAP and neurofibromatosis gene product activities. 1904555 1991
NOONAN SYNDROME 3
CUI: C1860991
Disease: NOONAN SYNDROME 3
0.700 GeneticVariation CLINVAR Biological and biochemical properties of human rasH genes mutated at codon 61. 3510078 1986