Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 33
rs531564 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 27
rs10719 0.677 0.680 5 31401340 3 prime UTR variant A/G;T snv 0.69 24