Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs267606900
MTPAP
1.000 10 30313926 missense variant T/C snv 1.4E-05 2
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
rs80356740
TARDBP
1.000 1 11022556 missense variant A/G snv 1.7E-05 2
rs2435211
MAPT
17 45985878 intron variant C/G;T snv 1
rs755221106
CACNA1G
0.851 0.040 17 50617560 missense variant G/A;T snv 4.0E-06 7
rs397515634
UCHL1-AS1 ; UCHL1
0.925 0.040 4 41256996 missense variant A/C snv 4.0E-06 3
rs1264519280
KHDRBS1
1.000 0.040 1 32014083 missense variant G/A snv 2
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
rs3857059
SNCA
1.000 0.040 4 89754087 intron variant A/G;T snv 2
rs104893768
RHO
0.807 0.080 3 129528801 missense variant C/A snv 11
rs398122403
SYNJ1
0.807 0.080 21 32695106 missense variant C/T snv 1.2E-05 11
rs431905511
SNCA
0.827 0.080 4 89828154 missense variant C/T snv 9
rs9468
MAPT
0.882 0.080 17 46024197 3 prime UTR variant T/C snv 0.15 0.14 6
rs2435200
MAPT
0.925 0.080 17 45994485 intron variant G/A snv 0.40 5
rs119467003
TDP1
0.882 0.080 14 89993420 missense variant A/G snv 2.1E-05 4
rs66468541
HSPD1
0.925 0.080 2 197497275 missense variant C/T snv 4
rs104893922
SMN1 ; SMN2
0.925 0.080 5 70946157 missense variant A/G snv 3
rs121912432
SOD1
0.925 0.080 21 31663832 missense variant C/G snv 4.0E-06 3
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
rs2275294
ZNF512B
0.925 0.080 20 63962894 intron variant G/A snv 0.25 3
rs537742207
MDH2
1.000 0.080 7 76054974 missense variant A/G snv 8.0E-06 7.0E-06 3
rs1360444859
SPSB3 ; IGFALS
1.000 0.080 16 1791721 missense variant T/C snv 1.2E-05 2