rs121913237, NRAS

N. diseases: 37
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.
Acute Undifferentiated Leukemia
CUI: C0280141
Disease: Acute Undifferentiated Leukemia
1 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.010 1.000 1 2015 2015
Chronic Lymphocytic Leukemia
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
228 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.010 1.000 1 1997 1997
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
240 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.010 1.000 1 2009 2009
Developmental Disabilities
CUI: C0008073
Disease: Developmental Disabilities
7 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.010 1.000 1 2011 2011
Diffuse Large B-Cell Lymphoma
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
71 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.010 1.000 1 1997 1997
Embryonal Rhabdomyosarcoma
CUI: C0206656
Disease: Embryonal Rhabdomyosarcoma
5 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.010 1.000 1 2013 2013
Hematologic Neoplasms
CUI: C0376545
Disease: Hematologic Neoplasms
37 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.010 1.000 1 2007 2007
Immunologic Deficiency Syndromes
CUI: C0021051
Disease: Immunologic Deficiency Syndromes
10 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.010 1.000 1 2011 2011
Leukemogenesis
CUI: C0598766
Disease: Leukemogenesis
12 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.010 1.000 1 2013 2013
Lymphoma
CUI: C0024299
Disease: Lymphoma
61 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.010 1.000 1 2011 2011
Malignant histiocytosis
CUI: C0019623
Disease: Malignant histiocytosis
1 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.010 1.000 1 2013 2013
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
135 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.010 1.000 1 2009 2009
Myeloproliferative disease
CUI: C0027022
Disease: Myeloproliferative disease
23 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.010 1.000 1 2011 2011
Nevus, Blue
CUI: C0206736
Disease: Nevus, Blue
1 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.010 1.000 1 2013 2013
Pre B-cell acute lymphoblastic leukemia
2 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.010 1.000 1 2014 2014
Precursor B-cell lymphoblastic leukemia
18 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.010 1.000 1 2014 2014
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
7 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.010 1.000 1 2011 2011
Undifferentiated leukemia
CUI: C1378511
Disease: Undifferentiated leukemia
1 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.010 1.000 1 2015 2015
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
159 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.020 1.000 2 2015 2016
Chronic myeloproliferative disorder
CUI: C1292778
Disease: Chronic myeloproliferative disorder
22 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.020 1.000 2 2011 2013
leukemia
CUI: C0023418
Disease: leukemia
76 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.020 1.000 2 2011 2015
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
226 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.700 9 2006 2016
Noonan Syndrome
CUI: C0028326
Disease: Noonan Syndrome
129 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.700 5 2004 2013
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
362 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.700 3 2003 2013
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
223 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.700 1 2016 2016