rs121913530, KRAS

N. diseases: 63
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.
Neoplasm, Residual
CUI: C0242596
Disease: Neoplasm, Residual
23 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.010 1.000 1 2019 2019
Neurilemmoma
CUI: C0027809
Disease: Neurilemmoma
11 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.010 1.000 1 2013 2013
Noonan Syndrome
CUI: C0028326
Disease: Noonan Syndrome
187 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.010 1.000 1 2007 2007
Papillary and follicular adenocarcinoma
2 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
Papillary carcinoma, clear cell
CUI: C1720430
Disease: Papillary carcinoma, clear cell
2 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
Poorly differentiated carcinoma
CUI: C0741899
Disease: Poorly differentiated carcinoma
2 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
Primary cholangiocarcinoma of intrahepatic biliary tract
10 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.010 1.000 1 2018 2018
Sebaceous adenoma
CUI: C1368816
Disease: Sebaceous adenoma
6 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.010 1.000 1 2016 2016
Secondary malignant neoplasm of bone
18 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.010 1.000 1 2016 2016
Secondary malignant neoplasm of liver
34 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.010 1.000 1 2018 2018
Split hand foot deformity 1
CUI: C2931019
Disease: Split hand foot deformity 1
8 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.010 1.000 1 2015 2015
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.010 1.000 1 2018 2018
Thyroid Nodule
CUI: C0040137
Disease: Thyroid Nodule
17 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.010 1.000 1 2006 2006
Adenomatous Polyposis Coli
CUI: C0032580
Disease: Adenomatous Polyposis Coli
237 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.020 1.000 2 2013 2015
Malignant neoplasm of colon and/or rectum
502 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.020 1.000 2 2019 2019
MUTYH-Associate Polyposis
CUI: C3272841
Disease: MUTYH-Associate Polyposis
36 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.020 1.000 2 2014 2015
polyps
CUI: C0032584
Disease: polyps
18 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.020 1.000 2 2014 2014
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.030 1.000 3 2014 2018
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.030 1.000 3 2014 2018
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
168 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.040 1.000 4 2016 2018
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.040 0.750 4 2015 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.040 1.000 4 2012 2020
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.050 1.000 5 2012 2020
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.070 1.000 7 2011 2019
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.100 1.000 15 2011 2019