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.
Juvenile Myelomonocytic Leukemia
CUI: C0349639
Disease: Juvenile Myelomonocytic Leukemia
70 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.820 1.000 10 2005 2019
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.800 0.933 15 2010 2019
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.800 0.923 13 1999 2020
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.790 1.000 26 2002 2019
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.740 1.000 4 2003 2019
Organoid Nevus Phakomatosis
CUI: C0265329
Disease: Organoid Nevus Phakomatosis
9 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.730 1.000 3 2012 2019
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.710 1.000 9 2005 2011
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.710 1.000 6 1987 2014
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.710 1.000 4 1987 2004
Arteriovenous Malformations, Cerebral
6 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.710 1.000 2 2019 2019
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
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.700 1.000 12 2005 2014
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.700 1.000 4 2007 2013
Gastrointestinal Stromal Tumors
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
154 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.700 1.000 2 2012 2014
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
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
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
14 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.700 0
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.100 0.970 67 1999 2020
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.100 0.857 14 2003 2016
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.100 1.000 13 2008 2019
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.100 0.909 11 2010 2019