rs121434595, NRAS

N. diseases: 19
Source: ALL
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
1962 0.708 0.320 1 114716124 missense variant C/A;G;T snv 0.800 0
Juvenile Myelomonocytic Leukemia
CUI: C0349639
Disease: Juvenile Myelomonocytic Leukemia
70 0.708 0.320 1 114716124 missense variant C/A;G;T snv 0.010 1.000 1 2012 2012
GIANT PIGMENTED HAIRY NEVUS
CUI: C1842036
Disease: GIANT PIGMENTED HAIRY NEVUS
6 0.708 0.320 1 114716124 missense variant C/A;G;T snv 0.800 1.000 2 2009 2013
melanoma
CUI: C0025202
Disease: melanoma
515 0.708 0.320 1 114716124 missense variant C/A;G;T snv 0.700 1.000 9 1989 2014
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.708 0.320 1 114716124 missense variant C/A;G;T snv 0.010 1.000 1 2014 2014
Stomach Neoplasms
CUI: C0038356
Disease: Stomach Neoplasms
55 0.708 0.320 1 114716124 missense variant C/A;G;T snv 0.700 1.000 1 2014 2014
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 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
248 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
235 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
6892 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
79 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
115 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
865 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
95 0.708 0.320 1 114716124 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Transitional cell carcinoma of bladder
158 0.708 0.320 1 114716124 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Benign melanocytic nevus
CUI: C1456781
Disease: Benign melanocytic nevus
20 0.708 0.320 1 114716124 missense variant C/A;G;T snv 0.020 1.000 2 2014 2017
Melanocytic nevus
CUI: C0027962
Disease: Melanocytic nevus
33 0.708 0.320 1 114716124 missense variant C/A;G;T snv 0.020 1.000 2 2014 2017
Nevus
CUI: C0027960
Disease: Nevus
43 0.708 0.320 1 114716124 missense variant C/A;G;T snv 0.020 1.000 2 2014 2017
Trichoepithelioma
CUI: C0349658
Disease: Trichoepithelioma
3 0.708 0.320 1 114716124 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017