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.
melanoma
CUI: C0025202
Disease: melanoma
515 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.010 1.000 1 2016 2016
Mucinous Adenocarcinoma
CUI: C0007130
Disease: Mucinous Adenocarcinoma
10 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.010 1.000 1 2014 2014
Multiple polyps
CUI: C0334108
Disease: Multiple polyps
32 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.010 1 2018 2018
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.010 1.000 1 2013 2013
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
CUI: C0206683
Disease: 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
CUI: C4284013
Disease: 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
CUI: C0153690
Disease: 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
CUI: C0494165
Disease: 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
Juvenile Myelomonocytic Leukemia
CUI: C0349639
Disease: Juvenile Myelomonocytic Leukemia
70 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.810 1.000 2 2007 2012
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.700 1.000 2 2008 2011
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
CUI: C4722085
Disease: 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
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.700 1.000 3 1987 2003
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