rs267601395, EZH2

N. diseases: 7
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.
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.925 0.160 7 148811636 missense variant A/G;T snv 0.010 1.000 1 2016 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.925 0.160 7 148811636 missense variant A/G;T snv 0.700 1.000 1 2016 2016
Lymphoma
CUI: C0024299
Disease: Lymphoma
91 0.925 0.160 7 148811636 missense variant A/G;T snv 0.700 1.000 1 2012 2012
Lymphoma, Non-Hodgkin, Familial
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
79 0.925 0.160 7 148811636 missense variant A/G;T snv 0.700 1.000 1 2016 2016
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.925 0.160 7 148811636 missense variant A/G;T snv 0.010 1.000 1 2012 2012
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.925 0.160 7 148811636 missense variant A/G;T snv 0.010 1.000 1 2018 2018
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.925 0.160 7 148811636 missense variant A/G;T snv 0.010 1.000 1 2012 2012