Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2435211
MAPT
17 45985878 intron variant C/G;T snv 1
rs1481950
ATP6V1H
1.000 0.080 8 53777725 intron variant C/A;G snv 2
rs371557337
DCTN4
1.000 0.040 5 150733475 start lost T/C;G snv 7.0E-06 2
rs63751177
GRN
1.000 0.120 17 44351438 stop gained G/A snv 2
rs1264519280
KHDRBS1
1.000 0.040 1 32014083 missense variant G/A snv 2
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
rs752933837
PRKCG
1.000 0.080 19 53906776 missense variant C/A snv 4.0E-06 1.4E-05 2
rs1428103360
SMN2
1.000 0.040 5 70070732 missense variant A/G snv 2
rs3857059
SNCA
1.000 0.040 4 89754087 intron variant A/G;T snv 2
rs1360444859
SPSB3 ; IGFALS
1.000 0.080 16 1791721 missense variant T/C snv 1.2E-05 2
rs80356740
TARDBP
1.000 1 11022556 missense variant A/G snv 1.7E-05 2
rs149215094
VAPB
1.000 0.080 20 58444203 missense variant G/A snv 5.6E-05 5.6E-05 2
rs387907043
DNAJC5
0.925 0.120 20 63930873 missense variant T/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
rs771845093
MFN2
0.925 0.160 1 12005903 missense variant G/A snv 8.0E-06 7.0E-06 3
rs1272951905
MTHFSD
0.925 0.160 16 86532210 missense variant C/T snv 2.1E-05 3
rs143061887
PSEN2
0.925 0.080 1 226881960 missense variant C/T snv 1.6E-05 5.6E-05 3
rs407135
SLC11A2
0.925 0.120 12 51017570 intron variant G/T snv 0.74 3
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
rs397515634
UCHL1-AS1 ; UCHL1
0.925 0.040 4 41256996 missense variant A/C snv 4.0E-06 3
rs1265011107
WDTC1
1.000 0.080 1 27283372 missense variant A/G snv 4.0E-06 3
rs2275294
ZNF512B
0.925 0.080 20 63962894 intron variant G/A snv 0.25 3