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: rs2929282
rs2929282
2 15 43953733 intron variant A/T snv 0.13 0.800 1.000 5 2010 2019
dbSNP: rs326
rs326
LPL
4 8 19961928 intron variant A/G snv 0.37 0.800 1.000 5 2008 2019
dbSNP: rs4420638
rs4420638
43 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.800 1.000 5 2007 2018
dbSNP: rs442177
rs442177
5 4 87109109 intron variant G/T snv 0.56 0.800 1.000 5 2010 2019
dbSNP: rs603446
rs603446
2 1.000 0.040 11 116783719 intron variant C/T snv 0.33 0.800 1.000 5 2011 2019
dbSNP: rs673548
rs673548
14 0.925 0.120 2 21014672 intron variant G/A;T snv 0.800 1.000 5 2009 2019
dbSNP: rs714052
rs714052
4 0.925 0.120 7 73450539 intron variant A/G snv 9.2E-02 0.800 1.000 5 2009 2019
dbSNP: rs780092
rs780092
10 0.827 0.160 2 27520287 intron variant A/G snv 0.18 0.800 1.000 5 2011 2019
dbSNP: rs9804646
rs9804646
3 11 116794363 upstream gene variant C/T snv 0.17 0.800 1.000 5 2012 2019
dbSNP: rs10761731
rs10761731
6 10 63267850 intron variant A/T snv 0.38 0.800 1.000 4 2010 2019
dbSNP: rs10808546
rs10808546
7 8 125483576 intron variant C/T snv 0.39 0.800 1.000 4 2012 2019
dbSNP: rs11613352
rs11613352
9 0.827 0.160 12 57398797 intron variant C/T snv 0.19 0.800 1.000 4 2010 2018
dbSNP: rs12130333
rs12130333
4 1.000 0.080 1 62726106 regulatory region variant C/T snv 0.16 0.800 1.000 4 2008 2019
dbSNP: rs12272004
rs12272004
5 1.000 0.040 11 116733008 TF binding site variant C/A snv 9.8E-02 0.800 1.000 4 2009 2019
dbSNP: rs1495741
rs1495741
9 0.827 0.240 8 18415371 regulatory region variant G/A snv 0.71 0.800 1.000 4 2010 2019
dbSNP: rs1532085
rs1532085
13 0.882 0.080 15 58391167 intron variant A/G;T snv 0.800 1.000 4 2010 2019
dbSNP: rs17321515
rs17321515
16 0.776 0.200 8 125474167 intron variant A/G snv 0.49 0.800 1.000 4 2008 2019
dbSNP: rs17410962
rs17410962
7 1.000 0.040 8 19990569 intergenic variant G/A snv 0.15 0.800 1.000 4 2012 2019
dbSNP: rs1748195
rs1748195
8 0.851 0.120 1 62583922 intron variant C/G;T snv 0.800 1.000 4 2008 2019
dbSNP: rs2144300
rs2144300
7 0.882 0.040 1 230159169 intron variant C/T snv 0.44 0.800 1.000 4 2008 2018
dbSNP: rs2238675
rs2238675
4 19 19225799 intron variant C/T snv 9.4E-02 0.800 1.000 4 2009 2019
dbSNP: rs2286276
rs2286276
5 0.925 0.120 7 73573024 non coding transcript exon variant C/T snv 0.28 0.800 1.000 4 2009 2019
dbSNP: rs268
rs268
LPL
41 0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 0.800 1.000 4 2012 2019
dbSNP: rs2954031
rs2954031
9 8 125479491 intron variant G/T snv 0.42 0.800 1.000 4 2012 2019
dbSNP: rs2972146
rs2972146
9 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 0.800 1.000 4 2010 2018