rs121913237, NRAS

N. diseases: 12
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.
Juvenile Myelomonocytic Leukemia
CUI: C0349639
Disease: Juvenile Myelomonocytic Leukemia
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.810 1.000 0 2007 2014
NEVUS, EPIDERMAL (disorder)
CUI: C0334082
Disease: NEVUS, EPIDERMAL (disorder)
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.800 1.000 0 2012 2012
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.740 1.000 9 1987 2017
melanoma
CUI: C0025202
Disease: melanoma
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.740 1.000 7 1989 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.710 1.000 1 2013 2016
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.700 1.000 9 2006 2016
Noonan Syndrome
CUI: C0028326
Disease: Noonan Syndrome
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.700 1.000 4 2004 2009
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.700 1.000 3 2002 2013
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.700 1.000 1 2016 2016
Malignant Uterine Corpus Neoplasm
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.700 1.000 1 2016 2016
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.700 1.000 1 2016 2016
MYELODYSPLASTIC SYNDROME
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.700 1.000 1 2016 2016