Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72824905
PLCG2
0.827 0.200 16 81908423 missense variant C/G;T snv 5.2E-03 6
rs1049564
PNP
0.882 0.160 14 20472447 missense variant G/A snv 0.19 0.21 6
rs63751068
PSEN1
0.827 0.120 14 73186920 missense variant G/C;T snv 6
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
rs2435200
MAPT
0.925 0.080 17 45994485 intron variant G/A snv 0.40 5
rs200161705
NEK1
0.882 0.160 4 169585374 missense variant C/A;T snv 6.0E-05; 2.3E-03 5
rs66468541
HSPD1
0.925 0.080 2 197497275 missense variant C/T snv 4
rs759504704
NARS2
0.882 0.200 11 78436786 missense variant C/A;T snv 4.0E-06; 4.0E-06 4
rs1178466848
PRNP
0.925 0.120 20 4699785 missense variant G/A snv 2.8E-05 4
rs119467003
TDP1
0.882 0.080 14 89993420 missense variant A/G snv 2.1E-05 4
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
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