Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs267601395
rs267601395
EZH2
0.925 0.160 7 148811636 missense variant A/G;T snv
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
Lymphoma, Non-Hodgkin, Familial 		0.700 1.000 1 2016 2016
dbSNP: rs267601395
rs267601395
EZH2
0.925 0.160 7 148811636 missense variant A/G;T snv
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma 		0.700 1.000 1 2016 2016
dbSNP: rs267601395
rs267601395
EZH2
0.925 0.160 7 148811636 missense variant A/G;T snv
CUI: C0024299
Disease: Lymphoma
Lymphoma 		0.700 1.000 1 2012 2012
dbSNP: rs267601395
rs267601395
EZH2
0.925 0.160 7 148811636 missense variant A/G;T snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.010 1.000 1 2016 2016
dbSNP: rs267601395
rs267601395
EZH2
0.925 0.160 7 148811636 missense variant A/G;T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.010 1.000 1 2012 2012
dbSNP: rs267601395
rs267601395
EZH2
0.925 0.160 7 148811636 missense variant A/G;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2018 2018
dbSNP: rs267601395
rs267601395
EZH2
0.925 0.160 7 148811636 missense variant A/G;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 1.000 1 2012 2012