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.
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
Adenoma
CUI: C0001430
Disease: Adenoma
103 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.010 1.000 1 2013 2013
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
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
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.730 1.000 5 2014 2019
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
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
Familial medullary thyroid carcinoma
45 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.010 1.000 1 2014 2014
Medullary carcinoma of thyroid
CUI: C0238462
Disease: Medullary carcinoma of thyroid
71 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.010 1.000 1 2014 2014
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
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
Endocardial Cushion Defects
CUI: C0014116
Disease: Endocardial Cushion Defects
4 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.010 1.000 1 2015 2015
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
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
ANOPHTHALMIA AND PULMONARY HYPOPLASIA
80 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.010 1.000 1 2016 2016
Conventional (Clear Cell) Renal Cell Carcinoma
222 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.010 1.000 1 2016 2016
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
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
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
Leukemia, Myelomonocytic, Chronic
CUI: C0023480
Disease: Leukemia, Myelomonocytic, Chronic
28 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
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