Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10010131 0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63 7
rs1004446 0.827 0.240 11 2148913 intron variant G/A snv 0.37 7
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs10084572 1.000 0.040 21 43992991 downstream gene variant T/A;C;G snv 3
rs10116772 0.882 0.080 9 4290541 intron variant C/A;T snv 4
rs1013773109 1.000 0.040 2 164497436 missense variant T/C snv 2.1E-05 2
rs1020608562 0.807 0.160 3 46373738 missense variant T/C snv 4.0E-06 9
rs1022113606 0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs10224002 0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs10224210 1.000 0.040 7 151716108 intron variant T/C snv 0.21 9
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1033656351 0.827 0.160 12 121232997 missense variant G/A snv 1.6E-05 2.8E-05 7
rs1036483919
GCK
0.925 0.080 7 44151050 missense variant A/G snv 4.0E-06 4
rs1036915 1.000 0.040 9 84822934 intron variant A/G snv 0.40 2
rs1037733674 0.882 0.120 2 162147429 missense variant T/C snv 1.4E-05 5
rs10401969 0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs1042488900 1.000 0.040 1 161802188 synonymous variant C/T snv 2
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042615 1.000 0.040 12 63150429 missense variant A/C;G;T snv 0.60; 1.2E-05 2
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1044250 0.807 0.240 19 8371280 missense variant C/T snv 0.30 0.29 12
rs1044498 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34