rs112445441, KRAS

N. diseases: 32
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.
Refractory Colorectal Carcinoma
CUI: C4688318
Disease: Refractory Colorectal Carcinoma
2 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.010 1.000 1 2010 2010
APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS
CUI: C1838329
Disease: APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS
5 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.010 1.000 1 2016 2016
Lymphoma, T-Cell, Cutaneous
CUI: C0079773
Disease: Lymphoma, T-Cell, Cutaneous
5 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.010 1.000 1 2011 2011
Sezary Syndrome
CUI: C0036920
Disease: Sezary Syndrome
7 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.010 1.000 1 2011 2011
Breast adenocarcinoma
CUI: C0858252
Disease: Breast adenocarcinoma
7 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.700 0
Mycosis Fungoides
CUI: C0026948
Disease: Mycosis Fungoides
8 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.010 1.000 1 2011 2011
Tumour budding
CUI: C4049272
Disease: Tumour budding
8 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.010 1.000 1 2015 2015
RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER
CUI: C2674723
Disease: RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER
14 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.700 0
Thymoma
CUI: C0040100
Disease: Thymoma
20 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.010 1.000 1 2009 2009
Autoimmune Lymphoproliferative Syndrome
CUI: C1328840
Disease: Autoimmune Lymphoproliferative Syndrome
22 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.010 1.000 1 2007 2007
Hypoglycemia
CUI: C0020615
Disease: Hypoglycemia
42 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.010 1.000 1 2005 2005
Hematologic Neoplasms
CUI: C0376545
Disease: Hematologic Neoplasms
60 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.010 1.000 1 2007 2007
Secondary malignant neoplasm of colon and/or rectum
CUI: C4721579
Disease: Secondary malignant neoplasm of colon and/or rectum
68 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.090 0.889 9 2010 2017
Juvenile Myelomonocytic Leukemia
CUI: C0349639
Disease: Juvenile Myelomonocytic Leukemia
70 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.810 1.000 1 2015 2015
Lymphoma, Follicular
CUI: C0024301
Disease: Lymphoma, Follicular
83 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.010 1.000 1 2018 2018
Secondary Neoplasm
CUI: C2939419
Disease: Secondary Neoplasm
85 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.010 1.000 1 2009 2009
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.700 1.000 4 2007 2013
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
168 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.020 1.000 2 2016 2016
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.010 1.000 1 2016 2016
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.040 1.000 4 2015 2019
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.020 1.000 2 2009 2020
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.040 1.000 4 2014 2019
melanoma
CUI: C0025202
Disease: melanoma
515 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.010 1.000 1 2019 2019
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.700 1.000 16 2005 2015
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.700 0