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: rs1800775
rs1800775
18 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 0.800 1.000 11 2007 2019
dbSNP: rs3764261
rs3764261
26 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 0.800 1.000 22 2008 2019
dbSNP: rs9989419
rs9989419
11 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 0.800 1.000 12 2008 2019
dbSNP: rs4846914
rs4846914
6 0.925 0.080 1 230159944 intron variant G/A snv 0.45 0.800 1.000 9 2008 2019
dbSNP: rs2156552
rs2156552
6 1.000 0.040 18 49655298 downstream gene variant A/G;T snv 0.800 1.000 7 2008 2019
dbSNP: rs5880
rs5880
10 0.827 0.040 16 56981179 missense variant G/C snv 5.2E-02 3.7E-02 0.800 1.000 7 2008 2019
dbSNP: rs10503669
rs10503669
8 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 0.800 1.000 6 2008 2019
dbSNP: rs17482753
rs17482753
8 1.000 0.080 8 19975135 regulatory region variant G/T snv 8.8E-02 0.800 1.000 5 2008 2019
dbSNP: rs1800588
rs1800588
16 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 0.800 1.000 5 2008 2019
dbSNP: rs1864163
rs1864163
10 0.882 0.120 16 56963321 intron variant G/A snv 0.26 0.800 1.000 5 2008 2019
dbSNP: rs2144300
rs2144300
7 0.882 0.040 1 230159169 intron variant C/T snv 0.44 0.800 1.000 5 2008 2018
dbSNP: rs328
rs328
LPL
19 0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 0.800 1.000 5 2008 2019
dbSNP: rs4775041
rs4775041
8 1.000 0.040 15 58382496 intron variant G/C snv 0.24 0.800 1.000 5 2008 2019
dbSNP: rs255052
rs255052
4 0.925 0.040 16 67991092 intron variant G/A snv 0.17 0.17 0.800 1.000 4 2008 2019
dbSNP: rs3890182
rs3890182
5 0.925 0.120 9 104885374 intron variant G/A;T snv 0.800 1.000 4 2008 2019
dbSNP: rs711752
rs711752
10 1.000 0.040 16 56962299 splice region variant G/A;C snv 0.800 1.000 4 2008 2016
dbSNP: rs9282541
rs9282541
13 0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 0.800 1.000 4 2008 2019
dbSNP: rs2338104
rs2338104
3 1.000 0.040 12 109457363 non coding transcript exon variant C/G snv 0.58 0.800 1.000 3 2008 2019
dbSNP: rs5882
rs5882
35 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.700 1.000 3 2008 2012
dbSNP: rs7205804
rs7205804
6 16 56970977 intron variant G/A snv 0.34 0.800 1.000 3 2008 2019
dbSNP: rs1800777
rs1800777
17 0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 0.700 1.000 2 2008 2012
dbSNP: rs11858164
rs11858164
3 15 58450532 intron variant T/G snv 0.39 0.700 1.000 1 2008 2008
dbSNP: rs1260326
rs1260326
81 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.700 1.000 1 2008 2008
dbSNP: rs12970134
rs12970134
13 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 0.700 1.000 1 2008 2008
dbSNP: rs4149268
rs4149268
4 1.000 0.040 9 104884939 intron variant C/T snv 0.46 0.800 1.000 1 2008 2008