Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs766001707
ATXN3
0.851 0.200 14 92096772 missense variant C/T snv 6
rs119467003
TDP1
0.882 0.080 14 89993420 missense variant A/G snv 2.1E-05 4
rs104893878
SNCA ; SNCA-AS1
0.732 0.160 4 89835580 missense variant C/G snv 21
rs104893875
SNCA
0.742 0.120 4 89828170 missense variant C/T snv 4.0E-06 13
rs431905511
SNCA
0.827 0.080 4 89828154 missense variant C/T snv 9
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs3857059
SNCA
1.000 0.040 4 89754087 intron variant A/G;T snv 2
rs1272951905
MTHFSD
0.925 0.160 16 86532210 missense variant C/T snv 2.1E-05 3
rs72824905
PLCG2
0.827 0.200 16 81908423 missense variant C/G;T snv 5.2E-03 6
rs759504704
NARS2
0.882 0.200 11 78436786 missense variant C/A;T snv 4.0E-06; 4.0E-06 4
rs537742207
MDH2
1.000 0.080 7 76054974 missense variant A/G snv 8.0E-06 7.0E-06 3
rs17125721
PSEN1
0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 14
rs63750311
PSEN1
0.790 0.240 14 73192647 missense variant A/C snv 8
rs63751068
PSEN1
0.827 0.120 14 73186920 missense variant G/C;T snv 6
rs104893922
SMN1 ; SMN2
0.925 0.080 5 70946157 missense variant A/G snv 3
rs1428103360
SMN2
1.000 0.040 5 70070732 missense variant A/G snv 2
rs2275294
ZNF512B
0.925 0.080 20 63962894 intron variant G/A snv 0.25 3
rs387907043
DNAJC5
0.925 0.120 20 63930873 missense variant T/A;G snv 4.0E-06 3
rs587777606
HNRNPUL2-BSCL2 ; BSCL2 ; LRRN4CL
0.851 0.160 11 62691300 stop gained G/A snv 4.0E-06 7.0E-06 6
rs149215094
VAPB
1.000 0.080 20 58444203 missense variant G/A snv 5.6E-05 5.6E-05 2
rs752933837
PRKCG
1.000 0.080 19 53906776 missense variant C/A snv 4.0E-06 1.4E-05 2
rs1481950
ATP6V1H
1.000 0.080 8 53777725 intron variant C/A;G snv 2
rs407135
SLC11A2
0.925 0.120 12 51017570 intron variant G/T snv 0.74 3
rs755221106
CACNA1G
0.851 0.040 17 50617560 missense variant G/A;T snv 4.0E-06 7
rs1178466848
PRNP
0.925 0.120 20 4699785 missense variant G/A snv 2.8E-05 4