Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750424
MAPT
0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30
rs33939927
LRRK2
0.708 0.120 12 40310434 missense variant C/A;G;T snv 4.0E-06; 1.2E-05 24
rs143624519
MAPT
0.724 0.240 17 45991484 missense variant G/A;T snv 1.5E-03; 1.2E-05 17
rs63751438
MAPT
0.776 0.120 17 46010388 missense variant C/T snv 16
rs242557
MAPT
0.752 0.200 17 45942346 intron variant G/A snv 0.36 12
rs76980269
NOS1
0.763 0.280 12 117330794 synonymous variant G/A snv 2.8E-05 4.2E-05 10
rs393152
LINC02210 ; LINC02210-CRHR1
0.851 0.160 17 45641777 non coding transcript exon variant A/G snv 0.18 0.29 7
rs9468
MAPT
0.882 0.080 17 46024197 3 prime UTR variant T/C snv 0.15 0.14 6
rs12185268
MAPT-AS1 ; SPPL2C
0.851 0.160 17 45846317 missense variant A/G snv 0.15 0.14 5
rs1768208
MOBP
0.851 0.200 3 39481512 intron variant T/C snv 0.76 4
rs643472 0.925 0.080 8 29296260 intergenic variant C/T snv 0.73 2
rs200769426
LRRK2
1.000 0.040 12 40321138 missense variant G/A snv 7.0E-06 1
rs777148159
MAPT
1.000 0.040 17 46024073 missense variant A/C snv 1.2E-05 1
rs963731
SOS1
1.000 0.040 2 38989732 intron variant T/C snv 0.90 1