Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs8070723
MAPT
0.851 0.240 17 46003698 intron variant A/G snv 0.18 7
rs387906711
UBQLN2
0.807 0.120 X 56565389 missense variant C/A;T snv 6.6E-06 6
rs80356718
TARDBP
0.827 0.120 1 11022209 missense variant A/G snv 7.6E-05 4.9E-05 5
rs1768208
MOBP
0.851 0.200 3 39481512 intron variant T/C snv 0.76 4
rs753325601
TREM2 ; LOC105375056
0.851 0.200 6 41161515 missense variant G/A snv 2.8E-05 7.0E-06 4
rs157590
TOMM40
0.882 0.160 19 44895459 intron variant A/C snv 0.60 3
rs1423300240
FUS
1.000 0.120 16 31184952 missense variant A/C;G snv 4.0E-06 1
rs374191107
FUS
1.000 0.120 16 31183984 missense variant C/T snv 1.6E-05 2.1E-05 1