rs121913240, KRAS

N. diseases: 24
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.
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.672 0.440 12 25227342 missense variant T/A;C;G snv 0.710 1.000 1 2017 2017
Medullary carcinoma of thyroid
CUI: C0238462
Disease: Medullary carcinoma of thyroid
71 0.672 0.440 12 25227342 missense variant T/A;C;G snv 0.710 1.000 1 2014 2014
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.672 0.440 12 25227342 missense variant T/A;C;G snv 0.700 1.000 9 2005 2014
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.672 0.440 12 25227342 missense variant T/A;C;G snv 0.700 1.000 4 2002 2008
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.672 0.440 12 25227342 missense variant T/A;C;G snv 0.700 1.000 4 2007 2013
Noonan Syndrome
CUI: C0028326
Disease: Noonan Syndrome
187 0.672 0.440 12 25227342 missense variant T/A;C;G snv 0.700 1.000 1 2010 2010
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.672 0.440 12 25227342 missense variant T/A;C;G snv 0.700 0
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.672 0.440 12 25227342 missense variant T/A;C;G snv 0.040 1.000 4 2014 2017
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.672 0.440 12 25227342 missense variant T/A;C;G snv 0.020 1.000 2 2016 2019
melanoma
CUI: C0025202
Disease: melanoma
515 0.672 0.440 12 25227342 missense variant T/A;C;G snv 0.020 1.000 2 2016 2018
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.672 0.440 12 25227342 missense variant T/A;C;G snv 0.020 1.000 2 2018 2019
Adult Diffuse Large B-Cell Lymphoma
CUI: C1332201
Disease: Adult Diffuse Large B-Cell Lymphoma
46 0.672 0.440 12 25227342 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 0.672 0.440 12 25227342 missense variant T/A;C;G snv 0.010 1.000 1 1997 1997
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.672 0.440 12 25227342 missense variant T/A;C;G snv 0.010 1.000 1 2015 2015
Chronic Lymphocytic Leukemia
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
291 0.672 0.440 12 25227342 missense variant T/A;C;G snv 0.010 1.000 1 1997 1997
Diffuse Large B-Cell Lymphoma
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
127 0.672 0.440 12 25227342 missense variant T/A;C;G snv 0.010 1.000 1 1997 1997
Familial medullary thyroid carcinoma
45 0.672 0.440 12 25227342 missense variant T/A;C;G snv 0.010 1.000 1 2014 2014
Inverted urothelial papilloma
CUI: C1334282
Disease: Inverted urothelial papilloma
3 0.672 0.440 12 25227342 missense variant T/A;C;G snv 0.010 1.000 1 2014 2014
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.672 0.440 12 25227342 missense variant T/A;C;G snv 0.010 1.000 1 2006 2006
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.672 0.440 12 25227342 missense variant T/A;C;G snv 0.010 1.000 1 2019 2019
Papilloma
CUI: C0030354
Disease: Papilloma
27 0.672 0.440 12 25227342 missense variant T/A;C;G snv 0.010 1.000 1 2014 2014
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.672 0.440 12 25227342 missense variant T/A;C;G snv 0.010 1.000 1 2019 2019
Skin Carcinogenesis
CUI: C1519346
Disease: Skin Carcinogenesis
7 0.672 0.440 12 25227342 missense variant T/A;C;G snv 0.010 1.000 1 2012 2012
Trichilemmoma
CUI: C0334263
Disease: Trichilemmoma
4 0.672 0.440 12 25227342 missense variant T/A;C;G snv 0.010 1.000 1 2014 2014