Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750311
PSEN1
0.790 0.240 14 73192647 missense variant A/C snv 8
rs397515634
UCHL1-AS1 ; UCHL1
0.925 0.040 4 41256996 missense variant A/C snv 4.0E-06 3
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1799990
PRNP
0.683 0.440 20 4699605 missense variant A/G snv 0.31 0.33 23
rs1990622 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 16
rs121912443
SOD1
0.732 0.160 21 31663857 missense variant A/G snv 15
rs17125721
PSEN1
0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 14
rs1052553
MAPT
0.827 0.200 17 45996523 synonymous variant A/G snv 0.14 0.15 8
rs35801418
LRRK2
0.827 0.120 12 40321114 missense variant A/G snv 7
rs119467003
TDP1
0.882 0.080 14 89993420 missense variant A/G snv 2.1E-05 4
rs104893922
SMN1 ; SMN2
0.925 0.080 5 70946157 missense variant A/G snv 3
rs1265011107
WDTC1
1.000 0.080 1 27283372 missense variant A/G snv 4.0E-06 3
rs537742207
MDH2
1.000 0.080 7 76054974 missense variant A/G snv 8.0E-06 7.0E-06 3
rs1428103360
SMN2
1.000 0.040 5 70070732 missense variant A/G snv 2
rs80356740
TARDBP
1.000 1 11022556 missense variant A/G snv 1.7E-05 2
rs156697
GSTO2
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35 25
rs3857059
SNCA
1.000 0.040 4 89754087 intron variant A/G;T snv 2
rs4925
GSTO1
0.677 0.560 10 104263031 missense variant C/A snv 0.25 0.23 28
rs104893768
RHO
0.807 0.080 3 129528801 missense variant C/A snv 11
rs5030732
UCHL1 ; UCHL1-AS1
0.790 0.160 4 41257616 missense variant C/A snv 0.24 0.16 10
rs752933837
PRKCG
1.000 0.080 19 53906776 missense variant C/A snv 4.0E-06 1.4E-05 2
rs3173615
TMEM106B
0.807 0.200 7 12229791 missense variant C/A;G snv 0.49 12
rs1481950
ATP6V1H
1.000 0.080 8 53777725 intron variant C/A;G snv 2
rs121909329
VCP
0.763 0.200 9 35065363 missense variant C/A;G;T snv 11