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.
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.700 1.000 4 2007 2013
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
Organoid Nevus Phakomatosis
CUI: C0265329
Disease: Organoid Nevus Phakomatosis
9 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
Secondary malignant neoplasm of colon and/or rectum
CUI: C4721579
Disease: 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
Arteriovenous Malformations, Cerebral
CUI: C0917804
Disease: Arteriovenous Malformations, Cerebral
6 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.710 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
CUI: C0003857
Disease: 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
Gastrointestinal Stromal Tumors
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
154 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.700 1.000 2 2012 2014
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
Malignant neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
315 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.020 1.000 2 2010 2011
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.020 1.000 2 2006 2018
Pancreatic Ductal Adenocarcinoma
CUI: C1335302
Disease: Pancreatic Ductal Adenocarcinoma
22 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.020 1.000 2 2013 2014
Pancreatic Intraductal Papillary Mucinous Neoplasm
CUI: C4511687
Disease: Pancreatic Intraductal Papillary Mucinous Neoplasm
8 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.020 1.000 2 2016 2016
Pancreatic Neoplasm
CUI: C0030297
Disease: Pancreatic Neoplasm
20 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.020 1.000 2 2014 2016
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.020 1.000 2 2016 2019
Secondary malignant neoplasm of lymph node
CUI: C0686619
Disease: Secondary malignant neoplasm of lymph node
188 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.020 1.000 2 2015 2015
Tumor Cell Invasion
CUI: C1269955
Disease: Tumor Cell Invasion
169 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.020 1.000 2 2012 2017