Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1022113606 0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1042579 0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10761741 1.000 0.040 10 63306426 intron variant G/T snv 0.38 4
rs10903323 0.807 0.160 8 10292057 intron variant A/G snv 0.15 8
rs11053646 0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs11234027 0.882 0.080 11 71523061 intron variant G/A snv 0.24 5
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1144507 0.925 0.080 11 123729767 missense variant A/C;G;T snv 0.68 2
rs114694170 1.000 0.040 5 88884379 non coding transcript exon variant T/C snv 3.6E-02 5
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs118204057
LPL
0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 16
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1239681664 0.716 0.320 9 104818690 synonymous variant A/G snv 7.0E-06 15
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs12713559 0.776 0.120 2 21006196 missense variant G/A snv 3.4E-04 5.0E-04 10
rs12794714 0.708 0.360 11 14892029 synonymous variant G/A snv 0.41 0.35 15
rs12817819 0.882 0.040 12 89645549 intron variant C/T snv 9.4E-02 3
rs1320702652 0.752 0.160 15 43824536 missense variant G/A snv 4.0E-06 11
rs138880920 1.000 0.040 9 104826957 missense variant C/G snv 3.3E-03 1.8E-03 1