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.
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
CUI: C4302356
Disease: 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
CUI: C2674723
Disease: 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
Adult Diffuse Large B-Cell Lymphoma
CUI: C1332201
Disease: Adult Diffuse Large B-Cell Lymphoma
46 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 1997 1997
B-CELL MALIGNANCY, LOW-GRADE
CUI: C1868683
Disease: B-CELL MALIGNANCY, LOW-GRADE
19 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 1997 1997
Chronic Lymphocytic Leukemia
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
291 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 1997 1997
Diffuse Large B-Cell Lymphoma
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
127 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 1997 1997
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
Gestational Trophoblastic Neoplasms
CUI: C1135868
Disease: Gestational Trophoblastic Neoplasms
7 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2004 2004
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2004 2004
Adult Glioblastoma
CUI: C0278878
Disease: Adult Glioblastoma
98 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1 2007 2007
Adult Pilocytic Astrocytoma
CUI: C0280781
Disease: Adult Pilocytic Astrocytoma
10 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2007 2007
Childhood Glioblastoma
CUI: C0280474
Disease: Childhood Glioblastoma
98 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1 2007 2007
Childhood Pilocytic Astrocytoma
CUI: C1332995
Disease: Childhood Pilocytic Astrocytoma
10 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2007 2007
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1 2007 2007
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
186 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1 2007 2007
Pilocytic Astrocytoma
CUI: C0334583
Disease: Pilocytic Astrocytoma
14 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2007 2007
Adult Lymphoma
CUI: C1332206
Disease: Adult Lymphoma
66 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2008 2008
Childhood Lymphoma
CUI: C1332979
Disease: Childhood Lymphoma
66 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2008 2008
Leukemia, T-Cell
CUI: C0023492
Disease: Leukemia, T-Cell
10 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2008 2008
Lymphoma
CUI: C0024299
Disease: Lymphoma
91 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2008 2008
Tumor Initiation
CUI: C0598935
Disease: Tumor Initiation
8 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2008 2008
Adenocarcinoma of colon
CUI: C0338106
Disease: Adenocarcinoma of colon
10 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2009 2009