Disease: Familial (FPAH)
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 42
rs33939927
LRRK2
0.708 0.120 12 40310434 missense variant C/A;G;T snv 4.0E-06; 1.2E-05 24
rs104893878
SNCA ; SNCA-AS1
0.732 0.160 4 89835580 missense variant C/G snv 21
rs63751438
MAPT
0.776 0.120 17 46010388 missense variant C/T snv 16
rs34778348
LRRK2 ; LOC105369736
0.742 0.120 12 40363526 missense variant G/A snv 1.7E-03 5.8E-04 15
rs104893875
SNCA
0.742 0.120 4 89828170 missense variant C/T snv 4.0E-06 13
rs767543900
MAPT
0.790 0.120 17 45971879 missense variant A/C;G snv 4.0E-06 10
rs188286943
VPS35
0.776 0.160 16 46662452 missense variant C/T snv 9
rs112176450
EIF4G1
0.807 0.080 3 184327401 missense variant G/A;T snv 2.1E-04 2.8E-04 7
rs63750416
MAPT
0.851 0.120 17 46010373 missense variant A/C snv 7
rs542171324
SNCA
0.851 0.160 4 89828148 missense variant G/A;C snv 8.0E-06; 4.0E-06 6
rs45539432
PINK1-AS ; PINK1
0.851 0.040 1 20649109 stop gained C/T snv 4.0E-05 3.5E-05 5
rs113388242
EIF4G1
0.925 0.080 3 184327376 missense variant C/T snv 4.0E-05 7.0E-05 3
rs774457232
EIF4G1
0.925 0.080 3 184331303 missense variant G/A;T snv 6.4E-05 3