LPAL2, lipoprotein(a) like 2, pseudogene, 80350

N. diseases: 53; N. variants: 12
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs3127599
rs3127599
0.925 0.040 6 160486102 intron variant C/T snv 0.28
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.710 1.000 2 2009 2012
dbSNP: rs12207325
rs12207325
6 160482879 intron variant G/A snv 7.1E-03
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement
0.700 1.000 1 2017 2017
dbSNP: rs12214416
rs12214416
1.000 0.040 6 160489485 intron variant T/A snv 3.8E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs147555597
rs147555597
1.000 0.040 6 160490564 intron variant G/A snv 5.5E-03
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement
0.700 1.000 1 2017 2017
dbSNP: rs147555597
rs147555597
1.000 0.040 6 160490564 intron variant G/A snv 5.5E-03
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs149565105
rs149565105
6 160457046 intron variant G/A snv 8.5E-03
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement
0.700 1.000 1 2015 2015
dbSNP: rs1510224
rs1510224
6 160473846 intron variant T/C snv 3.1E-02
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement
0.700 1.000 1 2017 2017
dbSNP: rs151181359
rs151181359
6 160513493 intron variant A/C snv 1.2E-02
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement
0.700 1.000 1 2017 2017
dbSNP: rs185414370
rs185414370
6 160468866 intron variant T/C snv 7.1E-03
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement
0.700 1.000 1 2015 2015
dbSNP: rs3123629
rs3123629
6 160485054 intron variant G/A snv 0.28
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs3127599
rs3127599
0.925 0.040 6 160486102 intron variant C/T snv 0.28
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.700 1.000 1 2009 2009
dbSNP: rs6902316
rs6902316
6 160472135 intron variant A/G;T snv
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement
0.700 1.000 1 2017 2017
dbSNP: rs1567438
rs1567438
0.925 0.200 6 160458599 intron variant T/C snv 0.25
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs1567438
rs1567438
0.925 0.200 6 160458599 intron variant T/C snv 0.25
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2010 2010
dbSNP: rs1567438
rs1567438
0.925 0.200 6 160458599 intron variant T/C snv 0.25
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs2457564
rs2457564
1.000 0.080 6 160456608 intron variant G/A snv 0.41
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs3123629
rs3123629
6 160485054 intron variant G/A snv 0.28
CUI: C0007273
Disease: Carotid Artery Diseases
Carotid Artery Diseases
Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2011 2011