rs121913238, KRAS

N. diseases: 17
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 Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.732 0.240 12 25227343 missense variant G/C;T snv 0.700 1.000 9 2005 2014
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.732 0.240 12 25227343 missense variant G/C;T snv 0.700 1.000 4 2007 2013
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.732 0.240 12 25227343 missense variant G/C;T snv 0.700 1.000 3 2002 2009
Secondary malignant neoplasm of colon and/or rectum
68 0.732 0.240 12 25227343 missense variant G/C;T snv 0.030 1.000 3 2013 2017
Adult Diffuse Large B-Cell Lymphoma
CUI: C1332201
Disease: Adult Diffuse Large B-Cell Lymphoma
46 0.732 0.240 12 25227343 missense variant G/C;T snv 0.010 1.000 1 2012 2012
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.732 0.240 12 25227343 missense variant G/C;T snv 0.010 1.000 1 2013 2013
Diffuse Large B-Cell Lymphoma
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
127 0.732 0.240 12 25227343 missense variant G/C;T snv 0.010 1.000 1 2012 2012
Histiocytosis, Langerhans-Cell
CUI: C0019621
Disease: Histiocytosis, Langerhans-Cell
12 0.732 0.240 12 25227343 missense variant G/C;T snv 0.010 1.000 1 2016 2016
Lymphoma, T-Cell, Cutaneous
CUI: C0079773
Disease: Lymphoma, T-Cell, Cutaneous
5 0.732 0.240 12 25227343 missense variant G/C;T snv 0.010 1.000 1 2011 2011
Malignant neoplasm of colon and/or rectum
502 0.732 0.240 12 25227343 missense variant G/C;T snv 0.010 1.000 1 2013 2013
Malignant neoplasm of soft tissue
CUI: C4551686
Disease: Malignant neoplasm of soft tissue
32 0.732 0.240 12 25227343 missense variant G/C;T snv 0.010 1.000 1 2013 2013
Mycosis Fungoides
CUI: C0026948
Disease: Mycosis Fungoides
8 0.732 0.240 12 25227343 missense variant G/C;T snv 0.010 1.000 1 2011 2011
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.732 0.240 12 25227343 missense variant G/C;T snv 0.010 1.000 1 2017 2017
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.732 0.240 12 25227343 missense variant G/C;T snv 0.010 1.000 1 2019 2019
Sarcoma
CUI: C1261473
Disease: Sarcoma
42 0.732 0.240 12 25227343 missense variant G/C;T snv 0.010 1.000 1 2013 2013
Sebaceous adenoma
CUI: C1368816
Disease: Sebaceous adenoma
6 0.732 0.240 12 25227343 missense variant G/C;T snv 0.010 1.000 1 2016 2016
Sezary Syndrome
CUI: C0036920
Disease: Sezary Syndrome
7 0.732 0.240 12 25227343 missense variant G/C;T snv 0.010 1.000 1 2011 2011