Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs1550117 0.790 0.320 2 25343038 upstream gene variant A/G;T snv 11
rs2241880 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 37
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs281864719
ALK
0.763 0.240 2 29220831 missense variant A/C;G;T snv 14
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs752021744 0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05 29
rs876658657 0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs121913682
KIT
0.605 0.400 4 54733167 missense variant A/G;T snv 52
rs4754 0.752 0.360 4 87981540 missense variant T/A;C snv 0.32 12
rs11134527 0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 33
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131