Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1977412 0.882 0.160 1 230716523 intron variant T/A;C snv 5
rs281865071 0.882 0.080 1 154571759 missense variant C/G;T snv 5
rs1397094538 0.925 0.120 1 23367044 missense variant A/T snv 4.0E-06 3
rs744373 0.851 0.160 2 127137039 downstream gene variant A/G snv 0.35 8
rs781587642 0.851 0.120 2 219250557 missense variant G/A;C snv 2.0E-05 6
rs104893877 0.614 0.360 4 89828149 missense variant C/T snv 59
rs1424266770 0.790 0.200 4 184632307 missense variant C/G snv 8.0E-06 10
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1554317002 0.724 0.440 7 39950821 frameshift variant C/- delins 45
rs80356702 0.882 0.120 7 143330868 missense variant G/A snv 4.0E-06 1.4E-05 9
rs370717845 0.763 0.320 8 43161462 missense variant G/A snv 33
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs2732260 0.882 0.200 8 33431749 intron variant G/A snv 8.4E-02 5
rs11142387 9 70383416 downstream gene variant A/C snv 0.49 7
rs1411832 1.000 0.040 10 106126497 intergenic variant C/T snv 0.10 2
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6277 0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs12273363 0.807 0.120 11 27723312 intron variant T/C snv 0.16 11
rs7127507 0.827 0.080 11 27693337 intron variant T/C snv 0.34 6
rs104894396 0.672 0.400 13 20189511 stop gained C/T snv 5.8E-04 1.1E-04 28
rs17125721 0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 14
rs63750577 0.827 0.120 14 73186881 missense variant C/T snv 8
rs63750852 0.790 0.120 14 73170998 missense variant G/A;T snv 8