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: rs1800610
rs1800610
TNF
0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.700 1.000 1 2011 2011
dbSNP: rs1800610
rs1800610
TNF
0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02
CUI: C0524909
Disease: Hepatitis B, Chronic
Hepatitis B, Chronic 		0.010 1.000 1 2017 2017
dbSNP: rs1800610
rs1800610
TNF
0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 1.000 1 2010 2010
dbSNP: rs1800610
rs1800610
TNF
0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.010 1.000 1 2008 2008
dbSNP: rs1800610
rs1800610
TNF
0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.010 1.000 1 2008 2008
dbSNP: rs1800610
rs1800610
TNF
0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02
CUI: C0030193
Disease: Pain
Pain 		0.010 1.000 1 2017 2017
dbSNP: rs1800610
rs1800610
TNF
0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.010 1.000 1 2010 2010