Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 42
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs76763715
GBA
0.658 0.520 1 155235843 missense variant T/C;G snv 2.3E-03 35
rs75932628
LOC105375056 ; TREM2
0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs63750424
MAPT
0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs7493
PON2
0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 24
rs74315401
PRNP
0.683 0.320 20 4699525 missense variant C/T snv 32
rs63750231
PSEN1
0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs1801132
ESR1
0.689 0.320 6 151944387 synonymous variant G/C snv 0.73 0.80 22
rs12976445
SPACA6 ; SPACA6P-AS ; MIRLET7E ; MIR125A
0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45 20
rs334558
LOC107986119 ; GSK3B
0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs63750215
PSEN2
0.701 0.240 1 226885603 missense variant A/T snv 19
rs2276109
MMP12
0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 18
rs33939927
LRRK2
0.708 0.120 12 40310434 missense variant C/A;G;T snv 4.0E-06; 1.2E-05 24
rs1805054
HTR6
0.708 0.200 1 19666020 synonymous variant C/T snv 0.15; 8.0E-06 0.16 17
rs5848
FAM171A2 ; GRN
0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 17
rs1345176461
LOC107984638 ; IRF2BPL
0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06 40
rs63750756
MAPT
0.716 0.200 17 46010324 missense variant T/G snv 2.6E-05 23
rs1289324472
GBA
0.716 0.400 1 155236354 missense variant T/C snv 1.4E-05 21
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 17
rs2695121
NR1H2
0.716 0.280 19 50377484 5 prime UTR variant T/C snv 0.70 16
rs652438
MMP12
0.716 0.400 11 102865911 missense variant T/C;G snv 7.1E-02; 2.5E-04 14
rs148881970
NAGLU
0.724 0.360 17 42543840 missense variant A/G snv 5.4E-05 1.3E-04 22