rs1800610, TNF

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.
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02 0.700 1.000 1 2011 2011
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02 0.010 1.000 1 2010 2010
Hepatitis B, Chronic
CUI: C0524909
Disease: Hepatitis B, Chronic
84 0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02 0.010 1.000 1 2017 2017
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02 0.010 1.000 1 2008 2008
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02 0.010 1.000 1 2010 2010
Pain
CUI: C0030193
Disease: Pain
196 0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02 0.010 1.000 1 2017 2017
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02 0.010 1.000 1 2008 2008