Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 79
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 221
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 169
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 33
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 127
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 117
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 55
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs3804100 0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs7758229 0.732 0.120 6 160419220 intron variant G/A;T snv 8
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs5273 0.827 0.080 1 186674636 missense variant A/C;G snv 4.0E-06; 7.6E-03 1.4E-02 6
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs1342387 0.776 0.120 1 202945228 intron variant T/C snv 0.53 12
rs12733285 0.776 0.120 1 202952912 intron variant C/T snv 0.26 12
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs712 0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 135
rs2297518 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 29
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 70