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: rs137852912
rs137852912
10 0.776 0.120 1 55057454 missense variant G/A;C;T snv 7.2E-05 0.740 1.000 4 2009 2018
dbSNP: rs104894503
rs104894503
9 0.776 0.160 15 63060899 missense variant G/A snv 1.6E-05 2.8E-05 0.030 1.000 3 1994 2012
dbSNP: rs12713559
rs12713559
10 0.776 0.120 2 21006196 missense variant G/A snv 3.4E-04 5.0E-04 0.030 1.000 3 1997 2006
dbSNP: rs144467873
rs144467873
9 0.776 0.120 2 21006289 missense variant G/A snv 1.7E-04 6.3E-05 0.700 1.000 1 2016 2016
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: rs374603772
rs374603772
9 0.776 0.160 1 55058630 missense variant C/T snv 4.4E-05 2.8E-05 0.010 1.000 1 2017 2017
dbSNP: rs879254850
rs879254850
9 0.776 0.160 19 11113365 missense variant A/G;T snv 4.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs139043155
rs139043155
10 0.790 0.200 19 11106668 missense variant T/A snv 3.2E-05 4.2E-05 0.800 1.000 33 1989 2017
dbSNP: rs750518671
rs750518671
9 0.790 0.200 19 11128085 missense variant G/A;C;T snv 8.0E-06 0.810 1.000 32 1989 2017
dbSNP: rs2228671
rs2228671
14 0.790 0.160 19 11100236 stop gained C/A;G;T snv 1.6E-05; 8.9E-02 0.800 1.000 31 1989 2017
dbSNP: rs879254925
rs879254925
8 0.790 0.120 19 11113680 missense variant G/T snv 0.020 1.000 2 2009 2013
dbSNP: rs104894724
rs104894724
8 0.790 0.120 19 55154146 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2003 2003
dbSNP: rs121909374
rs121909374
7 0.790 0.120 11 47342578 stop gained C/A;G snv 1.3E-05 0.010 1.000 1 1999 1999
dbSNP: rs1333047
rs1333047
9 0.790 0.240 9 22124505 intron variant A/T snv 0.63 0.010 1.000 1 2018 2018
dbSNP: rs373822756
rs373822756
8 0.807 0.200 19 11105568 missense variant A/G;T snv 5.2E-05 0.820 1.000 33 1989 2017
dbSNP: rs28942080
rs28942080
8 0.807 0.200 19 11113743 missense variant G/A;C;T snv 1.2E-05; 4.0E-06 0.810 1.000 32 1989 2017
dbSNP: rs11547917
rs11547917
7 0.807 0.200 19 11107491 stop gained C/A;G;T snv 0.800 1.000 31 1989 2017
dbSNP: rs104894502
rs104894502
6 0.807 0.120 15 63060915 missense variant A/G;T snv 0.030 1.000 3 1994 2012
dbSNP: rs564427867
rs564427867
6 0.807 0.160 1 55039931 missense variant G/A snv 2.8E-05 2.8E-05 0.020 1.000 2 2010 2014
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: rs121964856
rs121964856
8 0.807 0.120 1 201365297 missense variant C/A;T snv 0.010 1.000 1 1999 1999
dbSNP: rs121964858
rs121964858
6 0.807 0.120 1 201365244 missense variant A/C;G;T snv 0.010 1.000 1 1998 1998
dbSNP: rs28942111
rs28942111
7 0.807 0.120 1 55044016 missense variant T/A snv 0.010 1.000 1 2008 2008
dbSNP: rs515135
rs515135
9 0.807 0.160 2 21063185 intergenic variant T/C snv 0.73 0.010 1.000 1 2019 2019
dbSNP: rs879254693
rs879254693
7 0.807 0.160 19 11107424 missense variant T/A;C;G snv 0.010 1.000 1 2001 2001