rs121913529, KRAS

N. diseases: 135
Source: BEFREE ×
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.
Neoplasms
CUI: C0027651
Disease: Neoplasms
1571 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.100 0.970 67 1999 2020
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.100 0.857 14 2003 2016
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
183 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.100 1.000 13 2008 2019
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1186 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.800 0.923 13 1999 2020
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
995 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.800 0.933 12 2010 2019
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1000 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.100 0.909 11 2010 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.100 1.000 11 2009 2019
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.100 0.909 11 2010 2019
ANOPHTHALMIA AND PULMONARY HYPOPLASIA
CUI: C1832661
Disease: ANOPHTHALMIA AND PULMONARY HYPOPLASIA
62 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.100 1.000 10 2010 2018
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1441 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.100 1.000 10 2009 2019
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
601 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.790 1.000 9 2002 2019
Lung Neoplasms
CUI: C0024121
Disease: Lung Neoplasms
39 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.080 0.875 8 2008 2016
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
167 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.070 1.000 7 2012 2020
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.060 1.000 6 2012 2019
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.060 1.000 6 2009 2016
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
238 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.050 1.000 5 2003 2019
Tumor Progression
CUI: C0178874
Disease: Tumor Progression
72 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.050 0.800 5 2011 2017
melanoma
CUI: C0025202
Disease: melanoma
352 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.040 1.000 4 2013 2019
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
236 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.740 1.000 4 2003 2019
Rhabdomyosarcoma
CUI: C0035412
Disease: Rhabdomyosarcoma
17 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.040 1.000 4 2010 2018
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
85 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.030 1.000 3 2014 2017
Immunologic Deficiency Syndromes
CUI: C0021051
Disease: Immunologic Deficiency Syndromes
24 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.030 1.000 3 2005 2016
Organoid Nevus Phakomatosis
CUI: C0265329
Disease: Organoid Nevus Phakomatosis
5 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.730 1.000 3 2012 2019
Pancreatic intraepithelial neoplasia
CUI: C1301034
Disease: Pancreatic intraepithelial neoplasia
11 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.030 1.000 3 2007 2016
Precancerous Conditions
CUI: C0032927
Disease: Precancerous Conditions
18 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.030 1.000 3 2010 2015