rs11554290, NRAS

N. diseases: 59
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 lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
222 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.010 1.000 1 2016 2016
Adult Diffuse Large B-Cell Lymphoma
CUI: C1332201
Disease: Adult Diffuse Large B-Cell Lymphoma
46 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.010 1.000 1 1997 1997
B-CELL MALIGNANCY, LOW-GRADE
CUI: C1868683
Disease: B-CELL MALIGNANCY, LOW-GRADE
19 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.010 1.000 1 1997 1997
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.010 1.000 1 2016 2016
Carcinoma, Papillary
CUI: C0007133
Disease: Carcinoma, Papillary
9 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.010 1.000 1 2018 2018
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.010 1.000 1 2017 2017
Congenital chromosomal disease
CUI: C0008626
Disease: Congenital chromosomal disease
47 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.010 1.000 1 2018 2018
Differentiated Thyroid Gland Carcinoma
CUI: C1337013
Disease: Differentiated Thyroid Gland Carcinoma
80 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.010 1.000 1 2014 2014
Diffuse Large B-Cell Lymphoma
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
127 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.010 1.000 1 1997 1997
Dysplastic Nevus
CUI: C0205748
Disease: Dysplastic Nevus
7 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.010 1.000 1 2019 2019
Familial Hypophosphatemic Rickets
CUI: C3536983
Disease: Familial Hypophosphatemic Rickets
15 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.010 1.000 1 2017 2017
Follicular Variant Thyroid Gland Papillary Carcinoma
CUI: C3714651
Disease: Follicular Variant Thyroid Gland Papillary Carcinoma
13 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.010 1.000 1 2013 2013
Hypophosphatemic Rickets
CUI: C1704375
Disease: Hypophosphatemic Rickets
6 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.010 1.000 1 2017 2017
Invasive Cutaneous Melanoma
CUI: C1708565
Disease: Invasive Cutaneous Melanoma
7 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.010 1.000 1 2014 2014
Juvenile Myelomonocytic Leukemia
CUI: C0349639
Disease: Juvenile Myelomonocytic Leukemia
70 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.010 1.000 1 2016 2016
Malignant neoplasm of thyroid
CUI: C0007115
Disease: Malignant neoplasm of thyroid
103 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.010 1.000 1 2016 2016
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.010 1.000 1 2019 2019
Medullary carcinoma of thyroid
CUI: C0238462
Disease: Medullary carcinoma of thyroid
71 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.010 1.000 1 2017 2017
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.010 1.000 1 2017 2017
Papilloma
CUI: C0030354
Disease: Papilloma
27 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.010 1.000 1 2014 2014
Precursor Cell Lymphoblastic Leukemia Lymphoma
CUI: C1961102
Disease: Precursor Cell Lymphoblastic Leukemia Lymphoma
168 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.010 1.000 1 2016 2016
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.010 1.000 1 2019 2019
Secondary malignant neoplasm of bone
CUI: C0153690
Disease: Secondary malignant neoplasm of bone
18 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.010 1.000 1 2018 2018
Secondary Neoplasm
CUI: C2939419
Disease: Secondary Neoplasm
85 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.010 1.000 1 2017 2017
Skin Carcinogenesis
CUI: C1519346
Disease: Skin Carcinogenesis
7 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.010 1.000 1 2012 2012