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
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
Adrenocortical carcinoma
CUI: C0206686
Disease: Adrenocortical carcinoma
46 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.700 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
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
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
Chronic Lymphocytic Leukemia
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
291 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.710 1.000 2 1997 2016
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
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.700 1.000 8 2006 2016
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
Congenital melanocytic nevus
CUI: C1318558
Disease: Congenital melanocytic nevus
5 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.020 1.000 2 2016 2017
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
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 thyroid carcinoma
CUI: C0206682
Disease: Follicular thyroid carcinoma
28 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.020 1.000 2 2016 2018
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
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
235 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
GIANT PIGMENTED HAIRY NEVUS
CUI: C1842036
Disease: GIANT PIGMENTED HAIRY NEVUS
6 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.800 0
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
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