RIT1, Ras like without CAAX 1, 6016

N. diseases: 184; N. variants: 18
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1557962794
rs1557962794
0.882 0.160 1 155910693 missense variant T/G snv
CUI: C4551602
Disease: Noonan Syndrome 1
Noonan Syndrome 1
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases 0.700 0
dbSNP: rs672601334
rs672601334
0.752 0.400 1 155904798 missense variant G/C snv
CUI: C4551602
Disease: Noonan Syndrome 1
Noonan Syndrome 1
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases 0.700 0
dbSNP: rs672601335
rs672601335
0.882 0.160 1 155904456 missense variant C/G snv
CUI: C4551602
Disease: Noonan Syndrome 1
Noonan Syndrome 1
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases 0.700 0
dbSNP: rs730881014
rs730881014
0.776 0.360 1 155904494 stop gained A/C;G;T snv
CUI: C4551602
Disease: Noonan Syndrome 1
Noonan Syndrome 1
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases 0.700 0
dbSNP: rs869025191
rs869025191
0.827 0.160 1 155904739 missense variant C/A;G;T snv
CUI: C4551602
Disease: Noonan Syndrome 1
Noonan Syndrome 1
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases 0.700 0
dbSNP: rs869025195
rs869025195
0.790 0.280 1 155904493 missense variant T/G snv
CUI: C4551602
Disease: Noonan Syndrome 1
Noonan Syndrome 1
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases 0.700 0