rs267601394, EZH2

N. diseases: 8
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.
Lymphoma
CUI: C0024299
Disease: Lymphoma
91 0.807 0.200 7 148811635 missense variant T/A;G snv 0.720 1.000 4 2012 2016
Adult Lymphoma
CUI: C1332206
Disease: Adult Lymphoma
66 0.807 0.200 7 148811635 missense variant T/A;G snv 0.020 1.000 2 2014 2016
Childhood Lymphoma
CUI: C1332979
Disease: Childhood Lymphoma
66 0.807 0.200 7 148811635 missense variant T/A;G snv 0.020 1.000 2 2014 2016
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.807 0.200 7 148811635 missense variant T/A;G snv 0.010 1.000 1 2014 2014
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.807 0.200 7 148811635 missense variant T/A;G snv 0.700 1.000 1 2016 2016
Leukemogenesis
CUI: C0598766
Disease: Leukemogenesis
25 0.807 0.200 7 148811635 missense variant T/A;G snv 0.010 1.000 1 2014 2014
Lymphoma, Non-Hodgkin, Familial
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
79 0.807 0.200 7 148811635 missense variant T/A;G snv 0.700 1.000 1 2016 2016
melanoma
CUI: C0025202
Disease: melanoma
515 0.807 0.200 7 148811635 missense variant T/A;G snv 0.010 1.000 1 2016 2016