Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs75548401
GBA
0.882 0.160 1 155236246 missense variant G/A snv 5.9E-03 6.2E-03 6
rs1265011107
WDTC1
1.000 0.080 1 27283372 missense variant A/G snv 4.0E-06 3
rs143061887
PSEN2
0.925 0.080 1 226881960 missense variant C/T snv 1.6E-05 5.6E-05 3
rs771845093
MFN2
0.925 0.160 1 12005903 missense variant G/A snv 8.0E-06 7.0E-06 3
rs1264519280
KHDRBS1
1.000 0.040 1 32014083 missense variant G/A snv 2
rs80356740
TARDBP
1.000 1 11022556 missense variant A/G snv 1.7E-05 2
rs66468541
HSPD1
0.925 0.080 2 197497275 missense variant C/T snv 4
rs587778556
NFE2L2
2 177231705 missense variant G/A snv 3.2E-05 4.9E-05 2
rs755135182
NFE2L2
2 177231657 missense variant G/A snv 4.0E-06 2
rs104893768
RHO
0.807 0.080 3 129528801 missense variant C/A snv 11
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
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
rs1424266770
CASP3
0.790 0.200 4 184632307 missense variant C/G snv 8.0E-06 10
rs5030732
UCHL1 ; UCHL1-AS1
0.790 0.160 4 41257616 missense variant C/A snv 0.24 0.16 10
rs431905511
SNCA
0.827 0.080 4 89828154 missense variant C/T snv 9
rs121917767
UCHL1
0.827 0.120 4 41260751 missense variant C/A;G;T snv 4.0E-05; 4.0E-06; 2.0E-05 6
rs200161705
NEK1
0.882 0.160 4 169585374 missense variant C/A;T snv 6.0E-05; 2.3E-03 5
rs397515634
UCHL1-AS1 ; UCHL1
0.925 0.040 4 41256996 missense variant A/C snv 4.0E-06 3
rs3857059
SNCA
1.000 0.040 4 89754087 intron variant A/G;T snv 2
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
rs371557337
DCTN4
1.000 0.040 5 150733475 start lost T/C;G snv 7.0E-06 2