Source: ALL

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: rs9355296
rs9355296
LPA
6 160596961 intron variant G/A;T snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs9355296
rs9355296
LPA
6 160596961 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: rs10455872
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.030 0.333 3 2013 2017
dbSNP: rs10455872
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02
CUI: C0428791
Disease: Aortic valve calcification
Aortic valve calcification 		0.820 1.000 2 2013 2019
dbSNP: rs10455872
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.710 1.000 2 2013 2015
dbSNP: rs3798220
rs3798220
LPA
0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.020 0.500 2 2013 2014
dbSNP: rs55730499
rs55730499
LPA
1.000 0.040 6 160584578 intron variant C/T snv 4.5E-02
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement 		0.700 1.000 2 2013 2017
dbSNP: rs10455872
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction 		0.010 1.000 1 2013 2013
dbSNP: rs3798220
rs3798220
LPA
0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction 		0.010 1.000 1 2013 2013
dbSNP: rs3798220
rs3798220
LPA
0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02
CUI: C1842247
Disease: CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1 		0.700 1.000 1 2013 2013
dbSNP: rs6415084
rs6415084
LPA
1.000 0.040 6 160559298 intron variant T/C snv 0.57
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2013 2013
dbSNP: rs6919346
rs6919346
LPA
6 160539327 intron variant T/C snv 0.88
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs10455872
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02
CUI: C0003507
Disease: Aortic Valve Stenosis
Aortic Valve Stenosis 		0.030 1.000 3 2014 2019
dbSNP: rs41272114
rs41272114
LPA
1.000 0.040 6 160585045 splice donor variant C/A;T snv 1.2E-05; 4.1E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.710 1.000 2 2014 2018
dbSNP: rs10455872
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases 		0.010 1.000 1 2014 2014
dbSNP: rs10455872
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.700 1.000 1 2014 2014
dbSNP: rs10455872
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02
CUI: C0021775
Disease: Intermittent Claudication
Intermittent Claudication 		0.010 1.000 1 2014 2014
dbSNP: rs10455872
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02
CUI: C0333184
Disease: Calcific stenosis
Calcific stenosis 		0.010 1.000 1 2014 2014
dbSNP: rs9364559
rs9364559
LPA
1.000 0.040 6 160555116 intron variant A/G snv 0.16
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2014 2014
dbSNP: rs55730499
rs55730499
LPA
1.000 0.040 6 160584578 intron variant C/T snv 4.5E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 3 2015 2018
dbSNP: rs191555775
rs191555775
LPA
6 160584357 intron variant A/G;T snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 2 2015 2018
dbSNP: rs115848955
rs115848955
LPA
6 160610628 intron variant C/A;T snv
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement 		0.700 1.000 1 2015 2015
dbSNP: rs1367211
rs1367211
LPA
6 160661663 intron variant T/C snv 0.66
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement 		0.700 1.000 1 2015 2015
dbSNP: rs1801693
rs1801693
LPA
1.000 0.040 6 160548597 missense variant A/C;G snv 4.0E-06; 0.64
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2015 2015
dbSNP: rs3798221
rs3798221
LPA
6 160577116 intron variant G/T snv 0.21 0.19
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement 		0.700 1.000 1 2015 2015