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: rs1059611
rs1059611
LPL
3 8 19967052 3 prime UTR variant T/C snv 0.13 0.700 1.000 1 2009 2009
dbSNP: rs10889353
rs10889353
5 1 62652525 intron variant A/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs11075253
rs11075253
1 16 15054789 intron variant C/A snv 0.22 0.800 1.000 1 2012 2012
dbSNP: rs115136538
rs115136538
1 4 72456848 intron variant T/C snv 5.7E-03 0.800 1.000 1 2012 2012
dbSNP: rs115849089
rs115849089
7 8 20054859 intergenic variant G/A snv 9.8E-02 0.800 1.000 1 2012 2012
dbSNP: rs11644601
rs11644601
4 16 15078261 intron variant T/C snv 0.21 0.700 1.000 1 2016 2016
dbSNP: rs1167998
rs1167998
6 1 62465961 intron variant C/A snv 0.57 0.700 1.000 1 2009 2009
dbSNP: rs1168029
rs1168029
1 1 62503731 intron variant G/A;C snv 0.800 1.000 1 2012 2012
dbSNP: rs1168041
rs1168041
2 1 62494579 non coding transcript exon variant T/C snv 0.61 0.700 1.000 1 2016 2016
dbSNP: rs12713956
rs12713956
4 2 21018633 intron variant A/G snv 0.14 0.700 1.000 1 2013 2013
dbSNP: rs13247874
rs13247874
1 7 73596112 intron variant C/T snv 0.15 0.15 0.800 1.000 1 2012 2012
dbSNP: rs17111684
rs17111684
4 1 55159875 intron variant C/T snv 3.8E-02 0.700 1.000 1 2013 2013
dbSNP: rs17249141
rs17249141
4 19 11089332 upstream gene variant C/T snv 3.3E-03 0.700 1.000 1 2013 2013
dbSNP: rs17267292
rs17267292
2 13 92670893 intron variant T/C snv 0.22 0.700 1.000 1 2008 2008
dbSNP: rs17610395
rs17610395
1 11 68794860 missense variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs181807530
rs181807530
1 17 4871519 intron variant C/G snv 4.8E-03 0.700 1.000 1 2016 2016
dbSNP: rs186183604
rs186183604
1 11 67361262 intron variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs190121281
rs190121281
1 19 19141970 upstream gene variant G/A snv 3.5E-03 0.700 1.000 1 2016 2016
dbSNP: rs2229738
rs2229738
2 11 68794860 missense variant C/G;T snv 6.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs2575876
rs2575876
7 9 104903458 intron variant G/A snv 0.24 0.800 1.000 1 2012 2012
dbSNP: rs312985
rs312985
2 2 21155933 regulatory region variant A/G snv 0.75 0.700 1.000 1 2009 2009
dbSNP: rs331
rs331
LPL
4 8 19962894 intron variant G/A snv 0.30 0.700 1.000 1 2009 2009
dbSNP: rs35853021
rs35853021
1 15 58388444 intron variant G/T snv 0.38 0.800 1.000 1 2012 2012
dbSNP: rs506585
rs506585
4 2 21174310 intergenic variant G/A;C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs6065906
rs6065906
6 20 45925376 downstream gene variant T/A;C;G snv 0.700 1.000 1 2009 2009