Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2275294
ZNF512B
0.925 0.080 20 63962894 intron variant G/A snv 0.25 3
rs407135
SLC11A2
0.925 0.120 12 51017570 intron variant G/T snv 0.74 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
rs1481950
ATP6V1H
1.000 0.080 8 53777725 intron variant C/A;G snv 2
rs267606900
MTPAP
1.000 10 30313926 missense variant T/C snv 1.4E-05 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
rs63751177
GRN
1.000 0.120 17 44351438 stop gained G/A snv 2
rs2435211
MAPT
17 45985878 intron variant C/G;T snv 1
rs121912432
SOD1
0.925 0.080 21 31663832 missense variant C/G snv 4.0E-06 3
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
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
rs104893875
SNCA
0.742 0.120 4 89828170 missense variant C/T snv 4.0E-06 13
rs121909715
GSN
0.790 0.160 9 121310819 missense variant G/A;T snv 4.0E-06 8
rs587777606
HNRNPUL2-BSCL2 ; BSCL2 ; LRRN4CL
0.851 0.160 11 62691300 stop gained G/A snv 4.0E-06 7.0E-06 6
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs397515634
UCHL1-AS1 ; UCHL1
0.925 0.040 4 41256996 missense variant A/C snv 4.0E-06 3
rs759504704
NARS2
0.882 0.200 11 78436786 missense variant C/A;T snv 4.0E-06; 4.0E-06 4
rs1265011107
WDTC1
1.000 0.080 1 27283372 missense variant A/G snv 4.0E-06 3
rs752933837
PRKCG
1.000 0.080 19 53906776 missense variant C/A snv 4.0E-06 1.4E-05 2
rs387907043
DNAJC5
0.925 0.120 20 63930873 missense variant T/A;G snv 4.0E-06 3
rs755135182
NFE2L2
2 177231657 missense variant G/A snv 4.0E-06 2
rs755221106
CACNA1G
0.851 0.040 17 50617560 missense variant G/A;T snv 4.0E-06 7
rs771845093
MFN2
0.925 0.160 1 12005903 missense variant G/A snv 8.0E-06 7.0E-06 3