Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 42
rs63750687
PSEN1
0.752 0.200 14 73217137 missense variant C/A;G;T snv 33
rs74315401
PRNP
0.683 0.320 20 4699525 missense variant C/T snv 32
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs63750231
PSEN1
0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs1289324472
GBA
0.716 0.400 1 155236354 missense variant T/C snv 1.4E-05 21
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
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 20
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
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
rs5848
FAM171A2 ; GRN
0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 17
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
rs63751438
MAPT
0.776 0.120 17 46010388 missense variant C/T snv 16
rs63750083
PSEN1
0.732 0.160 14 73219177 missense variant C/A;T snv 13