Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs104893875 0.742 0.120 4 89828170 missense variant C/T snv 4.0E-06 13
rs104893877 0.614 0.360 4 89828149 missense variant C/T snv 59
rs104893878 0.732 0.160 4 89835580 missense variant C/G snv 21
rs104894685
FTL
0.925 0.120 19 48966317 missense variant G/A snv 4.0E-06 1.4E-05 4
rs1057518882
CYTB ; ND5 ; ND6
MT 14598 missense variant T/C snv 2
rs1057519629 16 2498332 missense variant C/G;T snv 2.1E-05 1
rs111501952 1.000 0.040 12 40310461 missense variant G/A snv 4.4E-05 7.7E-05 2
rs112176450 0.807 0.080 3 184327401 missense variant G/A;T snv 2.1E-04 2.8E-04 7
rs113388242 0.925 0.080 3 184327376 missense variant C/T snv 4.0E-05 7.0E-05 3
rs113994097 0.724 0.400 15 89323426 missense variant C/G snv 9.7E-04 7.9E-04 22
rs113994099 0.827 0.240 15 89320883 missense variant T/C snv 10
rs121908683 0.925 0.080 22 38115667 missense variant G/A snv 9.0E-06 2.1E-05 5
rs121917763
TH
0.925 0.040 11 2167896 missense variant A/G snv 1.2E-05 7.0E-06 5
rs121918304 0.925 0.080 22 32498453 stop gained C/A;T snv 4.0E-06; 4.0E-06 4
rs1224426272
CIT
0.925 0.040 12 119869138 missense variant C/T snv 6
rs1239756674 1.000 0.040 X 43743818 synonymous variant G/A snv 2
rs12817488 1.000 0.040 12 122811747 intron variant G/A snv 0.39 3
rs1289324472
GBA
0.716 0.400 1 155236354 missense variant T/C snv 1.4E-05 21
rs1290141855 1.000 0.040 16 55698539 missense variant T/C snv 4.0E-06 7.0E-06 3
rs137852538 0.925 0.080 X 78117385 missense variant A/T snv 3
rs139548132 1.000 1 119140608 missense variant A/C;G;T snv 3.2E-03; 1.6E-05; 4.0E-06 2
rs1417802320 1 7962861 missense variant A/T snv 4.0E-06 1
rs1426868527 1 20633841 missense variant G/A;T snv 3
rs143624519 0.724 0.240 17 45991484 missense variant G/A;T snv 1.5E-03; 1.2E-05 17