rs2069845, IL6

N. diseases: 8
Source: BEFREE ×
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.
Abnormal behavior
CUI: C0233514
Disease: Abnormal behavior
101 0.807 0.120 7 22730530 intron variant G/A snv 0.61 0.010 1.000 1 2018 2018
Benign Prostatic Hyperplasia
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
62 0.807 0.120 7 22730530 intron variant G/A snv 0.61 0.010 1.000 1 2019 2019
cervical cancer
CUI: C4048328
Disease: cervical cancer
257 0.807 0.120 7 22730530 intron variant G/A snv 0.61 0.010 1.000 1 2017 2017
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
266 0.807 0.120 7 22730530 intron variant G/A snv 0.61 0.010 1.000 1 2017 2017
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
861 0.807 0.120 7 22730530 intron variant G/A snv 0.61 0.010 1.000 1 2019 2019
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.807 0.120 7 22730530 intron variant G/A snv 0.61 0.010 1.000 1 2017 2017
Mental disorders
CUI: C0004936
Disease: Mental disorders
101 0.807 0.120 7 22730530 intron variant G/A snv 0.61 0.010 1.000 1 2018 2018
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
858 0.807 0.120 7 22730530 intron variant G/A snv 0.61 0.010 1.000 1 2019 2019