rs17231520, CETP

N. diseases: 9
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.
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
1440 0.851 0.240 16 56961915 upstream gene variant G/A snv 2.1E-02 0.800 1.000 4 2012 2019
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 0.851 0.240 16 56961915 upstream gene variant G/A snv 2.1E-02 0.700 1.000 2 2012 2012
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.851 0.240 16 56961915 upstream gene variant G/A snv 2.1E-02 0.010 1.000 1 2015 2015
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.851 0.240 16 56961915 upstream gene variant G/A snv 2.1E-02 0.010 1.000 1 2015 2015
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.851 0.240 16 56961915 upstream gene variant G/A snv 2.1E-02 0.010 1.000 1 2015 2015
Hemophilia B
CUI: C0008533
Disease: Hemophilia B
125 0.851 0.240 16 56961915 upstream gene variant G/A snv 2.1E-02 0.010 1.000 1 2015 2015
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.851 0.240 16 56961915 upstream gene variant G/A snv 2.1E-02 0.010 1.000 1 2015 2015
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.851 0.240 16 56961915 upstream gene variant G/A snv 2.1E-02 0.010 1.000 1 2015 2015
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.851 0.240 16 56961915 upstream gene variant G/A snv 2.1E-02 0.010 1.000 1 2015 2015