rs112445441, KRAS

N. diseases: 9
Source: CURATED ×
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
55 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.810 1.000 0 2015 2015
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
586 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.700 1.000 16 2005 2015
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6669 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.700 1.000 5 1987 2012
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
25 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.700 1.000 4 2007 2013
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
132 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.700 1.000 3 2002 2008
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
547 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.700 1.000 2 2008 2011
Breast adenocarcinoma
CUI: C0858252
Disease: Breast adenocarcinoma
5 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.700 0
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
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
44 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.700 0