rs121434595, NRAS

N. diseases: 13
Source: INFERRED ×
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
0.708 0.320 1 114716124 missense variant C/A;G;T snv 0.800 0
GIANT PIGMENTED HAIRY NEVUS
CUI: C1842036
Disease: GIANT PIGMENTED HAIRY NEVUS
0.708 0.320 1 114716124 missense variant C/A;G;T snv 0.800 1.000 0 2009 2013
melanoma
CUI: C0025202
Disease: melanoma
0.708 0.320 1 114716124 missense variant C/A;G;T snv 0.700 1.000 9 1989 2014
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
0.708 0.320 1 114716124 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
0.708 0.320 1 114716124 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
0.708 0.320 1 114716124 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
0.708 0.320 1 114716124 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Lymphoma, Non-Hodgkin, Familial
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
0.708 0.320 1 114716124 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Medulloblastoma
CUI: C0025149
Disease: Medulloblastoma
0.708 0.320 1 114716124 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
0.708 0.320 1 114716124 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
MYELODYSPLASTIC SYNDROME
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
0.708 0.320 1 114716124 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Stomach Neoplasms
CUI: C0038356
Disease: Stomach Neoplasms
0.708 0.320 1 114716124 missense variant C/A;G;T snv 0.700 1.000 1 2014 2014
Transitional cell carcinoma of bladder
0.708 0.320 1 114716124 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016