Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750680 1.000 0.080 14 73198076 missense variant T/C snv 2
rs772784579
GRN
1.000 0.040 17 44352387 missense variant C/A;T snv 4.0E-06; 4.0E-06 2
rs775809722 1.000 0.040 1 20633925 missense variant A/C;G snv 5.3E-06; 3.7E-05 2
rs1057519629 16 2498332 missense variant C/G;T snv 2.1E-05 1
rs1417802320 1 7962861 missense variant A/T snv 4.0E-06 1
rs41311141 22 32484019 synonymous variant A/G;T snv 3.4E-02 1
rs45467995 1 20649062 missense variant G/A snv 1
rs748705829 11 233109 missense variant T/C snv 8.0E-06 1
rs752804472 20 31484309 missense variant G/A;T snv 5.7E-06; 5.7E-06 1
rs756677845 1 20638074 frameshift variant G/- del 1
rs781652026 10 100989789 missense variant G/A;T snv 4.0E-06 1
rs1290141855 1.000 0.040 16 55698539 missense variant T/C snv 4.0E-06 7.0E-06 3
rs762999184 1.000 0.080 22 32478989 missense variant C/A;T snv 4.0E-06 7.0E-06 2
rs757199733
TTN
2 178799505 missense variant G/A snv 8.0E-06 7.0E-06 2
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
rs761807915 0.925 0.120 20 4699824 missense variant G/A snv 4.0E-06 7.0E-06 4
rs34995376 0.807 0.080 12 40310435 missense variant G/A snv 7.0E-06 7
rs74315356 0.925 0.040 1 20649054 stop gained G/A snv 4.0E-06 1.4E-05 3
rs1289324472
GBA
0.716 0.400 1 155236354 missense variant T/C snv 1.4E-05 21
rs34015634 0.851 0.120 12 40340380 missense variant T/C snv 3.2E-05 1.4E-05 8
rs104894685
FTL
0.925 0.120 19 48966317 missense variant G/A snv 4.0E-06 1.4E-05 4
rs121908683 0.925 0.080 22 38115667 missense variant G/A snv 9.0E-06 2.1E-05 5
rs758414077
FTL
19 48966681 synonymous variant G/A snv 8.0E-06 2.8E-05 1
rs45539432 0.851 0.040 1 20649109 stop gained C/T snv 4.0E-05 3.5E-05 5