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: rs1367117
rs1367117
8 1.000 0.080 2 21041028 missense variant G/A snv 0.26 0.24 0.700 1.000 1 2009 2009
dbSNP: rs1532085
rs1532085
13 0.882 0.080 15 58391167 intron variant A/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs1532624
rs1532624
12 0.851 0.160 16 56971567 intron variant C/A snv 0.34 0.700 1.000 1 2009 2009
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: rs1800775
rs1800775
18 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 0.700 1.000 1 2009 2009
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: rs1864163
rs1864163
10 0.882 0.120 16 56963321 intron variant G/A snv 0.26 0.700 1.000 1 2009 2009
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: 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: rs4245791
rs4245791
8 0.882 0.080 2 43847292 non coding transcript exon variant C/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs4299376
rs4299376
11 0.851 0.120 2 43845437 intron variant G/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs4803750
rs4803750
22 0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 0.700 1.000 1 2009 2009
dbSNP: rs4939883
rs4939883
5 1.000 0.040 18 49640844 TF binding site variant T/C;G snv 0.700 1.000 1 2009 2009
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
dbSNP: rs646776
rs646776
25 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.700 1.000 1 2009 2009
dbSNP: rs6511720
rs6511720
15 0.790 0.120 19 11091630 intron variant G/T snv 0.12 0.700 1.000 1 2009 2009
dbSNP: rs673548
rs673548
14 0.925 0.120 2 21014672 intron variant G/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs6754295
rs6754295
6 1.000 0.040 2 20983311 regulatory region variant T/G snv 0.27 0.700 1.000 1 2009 2009