Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 36
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 37
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 46
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs2228000
XPC
0.585 0.560 3 14158387 missense variant G/A snv 0.24 0.21 53
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 56
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 61
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 62
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 98
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 103
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 118
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134