rs3737787, TSTD1;USF1

N. diseases: 11
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.
HYPERLIPIDEMIA, FAMILIAL COMBINED, SUSCEPTIBILITY TO
3 0.763 0.280 1 161039733 3 prime UTR variant G/A snv 0.21 0.700 0
Hyperlipidemia, Familial Combined
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
28 0.763 0.280 1 161039733 3 prime UTR variant G/A snv 0.21 0.050 1.000 5 2005 2009
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.763 0.280 1 161039733 3 prime UTR variant G/A snv 0.21 0.040 1.000 4 2005 2008
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.763 0.280 1 161039733 3 prime UTR variant G/A snv 0.21 0.010 1.000 1 2019 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.763 0.280 1 161039733 3 prime UTR variant G/A snv 0.21 0.010 1.000 1 2015 2015
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.763 0.280 1 161039733 3 prime UTR variant G/A snv 0.21 0.010 1.000 1 2009 2009
Malignant neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
315 0.763 0.280 1 161039733 3 prime UTR variant G/A snv 0.21 0.010 1.000 1 2019 2019
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.763 0.280 1 161039733 3 prime UTR variant G/A snv 0.21 0.010 1.000 1 2005 2005
Obesity
CUI: C0028754
Disease: Obesity
1111 0.763 0.280 1 161039733 3 prime UTR variant G/A snv 0.21 0.010 1.000 1 2008 2008
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.763 0.280 1 161039733 3 prime UTR variant G/A snv 0.21 0.010 1.000 1 2019 2019
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.763 0.280 1 161039733 3 prime UTR variant G/A snv 0.21 0.010 1.000 1 2016 2016