Source: GWASDB

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: rs4773144
rs4773144
0.827 0.080 13 110308365 intron variant A/G snv 0.42
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.810 1.000 2 2011 2016
dbSNP: rs11617955
rs11617955
1.000 0.040 13 110165755 intron variant T/A snv 9.3E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.800 1.000 1 2013 2018
dbSNP: rs3809346
rs3809346
1.000 0.080 13 110308596 intron variant G/A;C snv
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.800 1.000 1 2011 2011
dbSNP: rs12873154
rs12873154
1.000 0.040 13 110268505 intron variant A/G snv 8.7E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1.000 1 2013 2013
dbSNP: rs3742207
rs3742207
0.925 0.120 13 110166251 missense variant T/A;G snv 2.8E-05; 0.30
CUI: C0599949
Disease: Arterial Stiffness
Arterial Stiffness
0.700 1.000 1 2009 2009
dbSNP: rs3809346
rs3809346
1.000 0.080 13 110308596 intron variant G/A;C snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 1.000 1 2011 2011
dbSNP: rs4773144
rs4773144
0.827 0.080 13 110308365 intron variant A/G snv 0.42
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1.000 1 2013 2013
dbSNP: rs4773144
rs4773144
0.827 0.080 13 110308365 intron variant A/G snv 0.42
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
0.700 1.000 1 2013 2013
dbSNP: rs494558
rs494558
13 110276815 intron variant C/T snv 0.90
CUI: C0162701
Disease: Polysomnography
Polysomnography
0.700 1.000 1 2012 2012
dbSNP: rs7330914
rs7330914
13 110274714 intron variant C/A snv 3.0E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs7330914
rs7330914
13 110274714 intron variant C/A snv 3.0E-02
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs7330914
rs7330914
13 110274714 intron variant C/A snv 3.0E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs7998875
rs7998875
13 110289053 intron variant G/A;T snv
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs7998875
rs7998875
13 110289053 intron variant G/A;T snv
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs7998875
rs7998875
13 110289053 intron variant G/A;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012