Source: BEFREE

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: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.830 1.000 3 2011 2018
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.830 1.000 3 2010 2019
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.810 1.000 1 2012 2012
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.730 1.000 3 2013 2018
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.710 1.000 1 2013 2019
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.020 1.000 2 2013 2018
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias
0.020 1.000 2 2010 2013
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.010 1.000 1 2013 2013
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
Diabetes Mellitus, Non-Insulin-Dependent
0.010 1.000 1 2016 2016
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0002895
Disease: Anemia, Sickle Cell
Anemia, Sickle Cell
0.010 1.000 1 2020 2020
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C2242712
Disease: Hyper LDL cholesterolaemia
Hyper LDL cholesterolaemia
0.010 1.000 1 2015 2015
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 1.000 1 2014 2014
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 1.000 1 2014 2014
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0410529
Disease: Hypochondroplasia (disorder)
Hypochondroplasia (disorder)
0.010 1.000 1 2014 2014