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.
increased risk of pancreatic cancer
CUI: C1842408
Disease: increased risk of pancreatic cancer
6 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.700 0
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.700 0
Nevus Sebaceus of Jadassohn
CUI: C4552097
Disease: Nevus Sebaceus of Jadassohn
7 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.700 0
Primary low grade serous adenocarcinoma of ovary
CUI: C4302356
Disease: Primary low grade serous adenocarcinoma of ovary
1 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.700 0
RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER
CUI: C2674723
Disease: RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER
14 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.700 0
NEVUS, EPIDERMAL (disorder)
CUI: C0334082
Disease: NEVUS, EPIDERMAL (disorder)
17 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.710 1.000 1 2010 2010
Stomach Neoplasms
CUI: C0038356
Disease: Stomach Neoplasms
55 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.710 1.000 1 2015 2015
Nevus sebaceous
CUI: C3854181
Disease: Nevus sebaceous
4 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.700 1.000 1 2013 2013
Acute monoblastic leukemia
CUI: C0457334
Disease: Acute monoblastic leukemia
5 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2014 2014
Acute monocytic leukemia
CUI: C0023465
Disease: Acute monocytic leukemia
22 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2014 2014
Adenoameloblastoma
CUI: C0334565
Disease: Adenoameloblastoma
2 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2019 2019
Adenocarcinoma of colon
CUI: C0338106
Disease: Adenocarcinoma of colon
10 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2009 2009
Adenocarcinoma of pancreas
CUI: C0281361
Disease: Adenocarcinoma of pancreas
138 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2017 2017
Adenocarcinoma, intestinal type
CUI: C0334279
Disease: Adenocarcinoma, intestinal type
2 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2018 2018
Adenoid Cystic Carcinoma
CUI: C0010606
Disease: Adenoid Cystic Carcinoma
30 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2009 2009
Adenoma
CUI: C0001430
Disease: Adenoma
103 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2012 2012
ADENOMAS AND ADENOCARCINOMAS
CUI: C1535510
Disease: ADENOMAS AND ADENOCARCINOMAS
2 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2013 2013
Adenomatous Polyposis Coli
CUI: C0032580
Disease: Adenomatous Polyposis Coli
237 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2016 2016
Adult Acute Monoblastic Leukemia
CUI: C0279629
Disease: Adult Acute Monoblastic Leukemia
5 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2014 2014
Adult Angiosarcoma
CUI: C0278592
Disease: Adult Angiosarcoma
1 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2016 2016
Adult Diffuse Large B-Cell Lymphoma
CUI: C1332201
Disease: Adult Diffuse Large B-Cell Lymphoma
46 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 1997 1997
Adult Glioblastoma
CUI: C0278878
Disease: Adult Glioblastoma
98 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1 2007 2007
Adult Liposarcoma
CUI: C0278608
Disease: Adult Liposarcoma
6 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2015 2015
Adult Lymphoma
CUI: C1332206
Disease: Adult Lymphoma
66 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2008 2008
Adult Pilocytic Astrocytoma
CUI: C0280781
Disease: Adult Pilocytic Astrocytoma
10 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2007 2007