Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs568408 0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16 29
rs752742313 0.637 0.320 3 138655502 missense variant C/T snv 1.2E-05 36
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 33
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs1273593548 0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs747126003 0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06 18
rs7025417 0.752 0.280 9 6240084 intron variant T/C;G snv 11
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs217727 0.641 0.480 11 1995678 non coding transcript exon variant G/A snv 0.20 34
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs1047768 0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs12894467 0.807 0.080 14 101041390 non coding transcript exon variant C/T snv 0.51 0.50 6
rs1760944 0.672 0.480 14 20454990 non coding transcript exon variant T/C;G snv 26
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242