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.
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.710 1.000 9 2005 2011
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
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.710 1.000 6 1987 2014
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
277 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.050 1.000 5 2003 2019
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
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 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
20 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.040 1.000 4 2010 2018
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.710 1.000 4 1987 2004
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