rs869025608, MAP2K1

N. diseases: 9
Source: CLINVAR ×
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.
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
211 0.763 0.400 15 66435117 missense variant G/C;T snv 0.700 1.000 2 2014 2016
Adenocarcinoma of prostate
CUI: C0007112
Disease: Adenocarcinoma of prostate
96 0.763 0.400 15 66435117 missense variant G/C;T snv 0.700 1.000 1 2016 2016
Cardio-facio-cutaneous syndrome
CUI: C1275081
Disease: Cardio-facio-cutaneous syndrome
70 0.763 0.400 15 66435117 missense variant G/C;T snv 0.700 1.000 1 2008 2008
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
153 0.763 0.400 15 66435117 missense variant G/C;T snv 0.700 1.000 1 2016 2016
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
188 0.763 0.400 15 66435117 missense variant G/C;T snv 0.700 1.000 1 2016 2016
Lymphoma, Non-Hodgkin, Familial
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
33 0.763 0.400 15 66435117 missense variant G/C;T snv 0.700 1.000 1 2016 2016
melanoma
CUI: C0025202
Disease: melanoma
129 0.763 0.400 15 66435117 missense variant G/C;T snv 0.700 1.000 1 2013 2013
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
82 0.763 0.400 15 66435117 missense variant G/C;T snv 0.700 1.000 1 2008 2008
Squamous cell carcinoma of the head and neck
179 0.763 0.400 15 66435117 missense variant G/C;T snv 0.700 1.000 1 2016 2016