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
rs113994099 0.827 0.240 15 89320883 missense variant T/C snv 10
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
rs143624519 0.724 0.240 17 45991484 missense variant G/A;T snv 1.5E-03; 1.2E-05 17
rs188286943 0.776 0.160 16 46662452 missense variant C/T snv 9
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs2421947 1.000 0.040 1 171863954 intron variant C/G;T snv 2
rs33939927 0.708 0.120 12 40310434 missense variant C/A;G;T snv 4.0E-06; 1.2E-05 24
rs35801418 0.827 0.120 12 40321114 missense variant A/G snv 7
rs367543041 0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 15
rs368134308 0.882 0.040 6 162443356 missense variant C/A;G;T snv 3.2E-05; 2.6E-04 4
rs421016
GBA
0.683 0.440 1 155235252 missense variant A/C;G snv 8.0E-06; 1.3E-03 30
rs542171324 0.851 0.160 4 89828148 missense variant G/A;C snv 8.0E-06; 4.0E-06 6
rs5569 0.742 0.280 16 55697923 synonymous variant G/A;C snv 0.31; 4.0E-06 19
rs767543900 0.790 0.120 17 45971879 missense variant A/C;G snv 4.0E-06 10
rs76763715
GBA
0.658 0.520 1 155235843 missense variant T/C;G snv 2.3E-03 35
rs774005786 0.790 0.080 1 7970951 missense variant G/A;T snv 3.9E-04; 2.0E-05 8
rs1290141855 1.000 0.040 16 55698539 missense variant T/C snv 4.0E-06 7.0E-06 3
rs121917763
TH
0.925 0.040 11 2167896 missense variant A/G snv 1.2E-05 7.0E-06 5
rs762472005 0.851 0.040 3 45722873 missense variant G/A snv 1.2E-05 7.0E-06 5