Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11542041 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 23
rs1314386070 0.827 0.240 8 90042766 missense variant T/C snv 1.4E-05 9
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs2071746 0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs213045 0.851 0.120 1 21290752 intron variant G/T snv 0.44 5
rs2227631 0.742 0.200 7 101126257 upstream gene variant A/G snv 0.54 13
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs405509 0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs4149313 0.763 0.240 9 104824472 missense variant T/C snv 9
rs646776 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116