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: rs10755578
rs10755578
LPA
0.925 0.040 6 160548706 intron variant C/G snv 0.44 0.42
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2009 2009
dbSNP: rs112842440
rs112842440
LPA
6 160534681 intron variant G/C;T snv
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement
0.700 1.000 1 2017 2017
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: rs116850263
rs116850263
LPA
6 160608638 intron variant T/A;C snv
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement
0.700 1.000 1 2017 2017
dbSNP: rs117026595
rs117026595
LPA
6 160647203 intron variant A/T snv 8.9E-03
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement
0.700 1.000 1 2017 2017
dbSNP: rs118039278
rs118039278
LPA
6 160564494 intron variant G/A snv 4.3E-02
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement
0.700 1.000 1 2017 2017
dbSNP: rs118039278
rs118039278
LPA
6 160564494 intron variant G/A snv 4.3E-02
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
0.700 1.000 1 2019 2019
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: rs140570886
rs140570886
LPA
1.000 0.040 6 160591981 intron variant T/C snv 2.8E-02
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement
0.700 1.000 1 2017 2017
dbSNP: rs140570886
rs140570886
LPA
1.000 0.040 6 160591981 intron variant T/C snv 2.8E-02
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2019 2019
dbSNP: rs141550222
rs141550222
LPA
6 160570969 intron variant C/G snv 2.1E-02
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement
0.700 1.000 1 2017 2017
dbSNP: rs145470851
rs145470851
LPA
6 160583319 intron variant G/A snv 4.9E-03
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement
0.700 1.000 1 2017 2017
dbSNP: rs185882981
rs185882981
LPA
6 160590288 intron variant T/A;C snv
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement
0.700 1.000 1 2018 2018
dbSNP: rs185934663
rs185934663
LPA
6 160646897 intron variant T/G snv 8.7E-03
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement
0.700 1.000 1 2017 2017
dbSNP: rs188974863
rs188974863
LPA
6 160653951 intron variant T/A;G snv
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement
0.700 1.000 1 2017 2017
dbSNP: rs191555775
rs191555775
LPA
6 160584357 intron variant A/G;T snv
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs191555775
rs191555775
LPA
6 160584357 intron variant A/G;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs3798220
rs3798220
LPA
0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs3798220
rs3798220
LPA
0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs3798220
rs3798220
LPA
0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
0.700 1.000 1 2013 2013
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
dbSNP: rs41259144
rs41259144
LPA
6 160601075 missense variant C/A;T snv 1.6E-05; 7.7E-03
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement
0.700 1.000 1 2017 2017
dbSNP: rs41265930
rs41265930
LPA
6 160543103 intron variant T/C snv 3.6E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2018 2018
dbSNP: rs41267807
rs41267807
LPA
6 160531784 missense variant T/C snv 1.0E-02 1.0E-02
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement
0.700 1.000 1 2017 2017
dbSNP: rs41267809
rs41267809
LPA
6 160532610 missense variant A/G;T snv 2.1E-02; 1.2E-05
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement
0.700 1.000 1 2017 2017