Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1989969
VDR
0.827 0.120 12 47884227 intron variant A/C;G;T snv 0.60 8
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 29
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
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs759412116 0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 55
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1289543302 0.763 0.440 7 87536472 missense variant C/T snv 12
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs2107425 0.732 0.280 11 1999845 intron variant C/T snv 16
rs2294008
PSCA ; JRK
0.672 0.320 8 142680513 5 prime UTR variant C/T snv 0.46 0.45 28
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48