rs121913529, KRAS

N. diseases: 144
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.
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
80 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
1641 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.100 1.000 10 2009 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
168 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
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
277 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
515 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.040 1.000 4 2013 2019
Rhabdomyosarcoma
CUI: C0035412
Disease: Rhabdomyosarcoma
20 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
204 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
31 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.030 1.000 3 2005 2016
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
Secondary malignant neoplasm of colon and/or rectum
68 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.030 1.000 3 2016 2019
Secondary Neoplasm
CUI: C2939419
Disease: Secondary Neoplasm
85 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.030 1.000 3 2009 2016
Adult Rhabdomyosarcoma
CUI: C0279550
Disease: Adult Rhabdomyosarcoma
12 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.020 1.000 2 2010 2013
Arteriovenous hemangioma
CUI: C0334533
Disease: Arteriovenous hemangioma
14 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.020 1.000 2 2019 2019
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.020 1.000 2 2014 2016
Childhood Rhabdomyosarcoma
CUI: C0220611
Disease: Childhood Rhabdomyosarcoma
12 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.020 1.000 2 2010 2013
Congenital arteriovenous malformation
23 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.020 1.000 2 2019 2019
Ductal Carcinoma
CUI: C1176475
Disease: Ductal Carcinoma
11 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.020 1.000 2 2015 2016
leukemia
CUI: C0023418
Disease: leukemia
144 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.020 1.000 2 2014 2016