Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs10680577 0.776 0.160 19 40798690 intron variant -/TACT delins 10
rs1057519729 0.827 0.080 15 66435113 missense variant A/C snv 6
rs12951053 0.732 0.160 17 7674089 intron variant A/C snv 0.10 14
rs213210 0.742 0.240 6 33208047 upstream gene variant A/C;G snv 11
rs1057519975 0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs3756712 0.790 0.160 5 308981 non coding transcript exon variant A/C;T snv 10
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs2241880 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 37
rs2307486 0.790 0.240 14 20456045 missense variant A/G snv 7.4E-03 2.1E-03 7
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs33917957
MET
0.790 0.120 7 116700208 missense variant A/G snv 2.7E-02 1.8E-02 10