Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10455872
rs10455872
LPA
33 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.010 1.000 1 2019 2019
dbSNP: rs104894724
rs104894724
TNNI3
8 0.790 0.120 19 55154146 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2003 2003
dbSNP: rs11053646
rs11053646
OLR1
18 0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 0.010 1.000 1 2017 2017
dbSNP: rs11542041
rs11542041
APOE
23 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 0.010 1.000 1 2014 2014
dbSNP: rs11613352
rs11613352
R3HDM2
9 0.827 0.160 12 57398797 intron variant C/T snv 0.19 0.010 1.000 1 2015 2015
dbSNP: rs118204057
rs118204057
LPL
16 0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 0.010 1.000 1 1998 1998
dbSNP: rs118204060
rs118204060
LPL
9 0.807 0.160 8 19954279 missense variant C/T snv 4.0E-05 1.4E-05 0.010 1.000 1 1998 1998
dbSNP: rs1217691063
rs1217691063
MTHFR
614 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.010 1.000 1 1998 1998
dbSNP: rs121909374
rs121909374
MYBPC3
7 0.790 0.120 11 47342578 stop gained C/A;G snv 1.3E-05 0.010 1.000 1 1999 1999
dbSNP: rs121964856
rs121964856
TNNT2
8 0.807 0.120 1 201365297 missense variant C/A;T snv 0.010 1.000 1 1999 1999
dbSNP: rs121964858
rs121964858
TNNT2
6 0.807 0.120 1 201365244 missense variant A/C;G;T snv 0.010 1.000 1 1998 1998
dbSNP: rs1226992086
rs1226992086
APOB
2 0.925 0.080 2 21041055 missense variant C/G;T snv 4.0E-06 0.010 1.000 1 2003 2003
dbSNP: rs1240681880
rs1240681880
DNAH8
3 0.882 0.160 6 38722870 missense variant G/A snv 2.1E-05 0.010 1.000 1 2005 2005
dbSNP: rs12526453
rs12526453
PHACTR1
5 0.827 0.160 6 12927312 intron variant C/G snv 0.27 0.010 1.000 1 2019 2019
dbSNP: rs1256476287
rs1256476287
LDLR
2 0.925 0.080 19 11106605 missense variant T/A snv 4.0E-06 0.010 1.000 1 2000 2000
dbSNP: rs12720762
rs12720762
APOB
2 0.925 0.080 2 21043787 intron variant C/G snv 4.8E-03 0.010 1.000 1 2013 2013
dbSNP: rs13306505
rs13306505
LDLR
2 0.925 0.080 19 11131312 missense variant C/A;T snv 5.2E-05 0.010 1.000 1 2020 2020
dbSNP: rs1333047
rs1333047
CDKN2B-AS1
9 0.790 0.240 9 22124505 intron variant A/T snv 0.63 0.010 1.000 1 2018 2018
dbSNP: rs143394031
rs143394031
PCSK9
2 0.925 0.080 1 55058640 missense variant G/A;C;T snv 1.6E-05; 4.9E-05; 1.6E-05 0.010 1.000 1 2019 2019
dbSNP: rs151009667
rs151009667
APOB
2 0.925 0.080 2 21011802 missense variant C/T snv 1.3E-03 1.4E-03 0.010 < 0.001 1 2019 2019
dbSNP: rs1553135971
rs1553135971
PCSK9
3 0.882 0.080 1 55044021 missense variant A/G snv 0.010 1.000 1 2008 2008
dbSNP: rs17321515
rs17321515 		16 0.776 0.200 8 125474167 intron variant A/G snv 0.49 0.010 1.000 1 2011 2011
dbSNP: rs1799983
rs1799983
NOS3
246 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2002 2002
dbSNP: rs1801275
rs1801275
IL4R
58 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 0.010 1.000 1 2015 2015
dbSNP: rs200353509
rs200353509
APOB
4 0.882 0.120 2 21035701 missense variant G/A;C;T snv 4.0E-06; 6.0E-05 0.010 1.000 1 1998 1998