rs121913237, NRAS

N. diseases: 50
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.
Pre B-cell acute lymphoblastic leukemia
CUI: C0349636
Disease: Pre B-cell acute lymphoblastic leukemia
5 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.010 1.000 1 2014 2014
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
CUI: C1961099
Disease: Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
23 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.010 1.000 1 2011 2011
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.010 1.000 1 2014 2014
Seborrheic keratosis
CUI: C0022603
Disease: Seborrheic keratosis
21 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.010 1.000 1 2014 2014
Tumor Cell Invasion
CUI: C1269955
Disease: Tumor Cell Invasion
169 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.010 1.000 1 2017 2017
Tumour budding
CUI: C4049272
Disease: Tumour budding
8 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.010 1.000 1 2017 2017
Undifferentiated leukemia
CUI: C1378511
Disease: Undifferentiated leukemia
2 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.010 1.000 1 2014 2014
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.020 1.000 2 2015 2015
leukemia
CUI: C0023418
Disease: leukemia
144 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.020 1.000 2 2011 2014
Leukemogenesis
CUI: C0598766
Disease: Leukemogenesis
25 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.020 1.000 2 2013 2019
Myeloproliferative disease
CUI: C0027022
Disease: Myeloproliferative disease
43 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.030 1.000 3 2011 2017
Chronic myeloproliferative disorder
CUI: C1292778
Disease: Chronic myeloproliferative disorder
47 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.040 1.000 4 2011 2017
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.100 1.000 10 2010 2020
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 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
187 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
712 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
235 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
152 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
865 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
95 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.700 1.000 1 2016 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.710 1.000 2 2013 2016
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.740 1.000 13 1987 2017
melanoma
CUI: C0025202
Disease: melanoma
515 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.740 1.000 11 1989 2016
NEVUS, EPIDERMAL (disorder)
CUI: C0334082
Disease: NEVUS, EPIDERMAL (disorder)
17 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.800 1.000 1 2012 2012
Juvenile Myelomonocytic Leukemia
CUI: C0349639
Disease: Juvenile Myelomonocytic Leukemia
70 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.810 1.000 3 2007 2014