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.
Nevus sebaceous
CUI: C3854181
Disease: Nevus sebaceous
9 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.700 0
Nevus, Keratinocytic, Nonepidermolytic
6 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.700 0
Woolly hair nevus
CUI: C0343114
Disease: Woolly hair nevus
6 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.700 0
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
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
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
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
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
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
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
Leukemia, Myelomonocytic, Chronic
CUI: C0023480
Disease: Leukemia, Myelomonocytic, Chronic
36 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.710 1.000 1 2011 2011
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
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
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
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
Juvenile Myelomonocytic Leukemia
CUI: C0349639
Disease: Juvenile Myelomonocytic Leukemia
37 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.810 1.000 4 2007 2013
NEVUS, EPIDERMAL (disorder)
CUI: C0334082
Disease: NEVUS, EPIDERMAL (disorder)
12 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.800 3 2007 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
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
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
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
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
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
melanoma
CUI: C0025202
Disease: melanoma
389 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 0.740 0.750 11 1989 2014
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