Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs886039227 0.925 0.200 2 74378123 missense variant A/C snv 4
rs80338892
TH
1.000 0.040 11 2167905 missense variant C/T snv 1.1E-04 1.4E-04 3
rs781652026 10 100989789 missense variant G/A;T snv 4.0E-06 1
rs781442277 1.000 0.040 2 24793223 missense variant C/T snv 4.0E-06; 1.2E-05 3
rs775809722 1.000 0.040 1 20633925 missense variant A/C;G snv 5.3E-06; 3.7E-05 2
rs774457232 0.925 0.080 3 184331303 missense variant G/A;T snv 6.4E-05 3
rs774005786 0.790 0.080 1 7970951 missense variant G/A;T snv 3.9E-04; 2.0E-05 8
rs772784579
GRN
1.000 0.040 17 44352387 missense variant C/A;T snv 4.0E-06; 4.0E-06 2
rs76763715
GBA
0.658 0.520 1 155235843 missense variant T/C;G snv 2.3E-03 35
rs767543900 0.790 0.120 17 45971879 missense variant A/C;G snv 4.0E-06 10
rs762999184 1.000 0.080 22 32478989 missense variant C/A;T snv 4.0E-06 7.0E-06 2
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
rs758414077
FTL
19 48966681 synonymous variant G/A snv 8.0E-06 2.8E-05 1
rs757199733
TTN
2 178799505 missense variant G/A snv 8.0E-06 7.0E-06 2
rs756677845 1 20638074 frameshift variant G/- del 1
rs752804472 20 31484309 missense variant G/A;T snv 5.7E-06; 5.7E-06 1
rs752078407 1.000 0.080 20 3910806 missense variant A/T snv 6.4E-05 3.5E-05 3
rs748705829 11 233109 missense variant T/C snv 8.0E-06 1
rs74315414 0.882 0.200 20 4699533 missense variant C/A;T snv 4.0E-06 5
rs74315360 0.925 0.040 1 20638104 missense variant C/A snv 3
rs74315356 0.925 0.040 1 20649054 stop gained G/A snv 4.0E-06 1.4E-05 3
rs71653619 1.000 0.040 1 7970934 missense variant G/A snv 7.9E-03 7.0E-03 4
rs63751438 0.776 0.120 17 46010388 missense variant C/T snv 16
rs63751273 0.645 0.280 17 46010389 missense variant C/T snv 42