Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs242557
MAPT
0.752 0.200 17 45942346 intron variant G/A snv 0.36 12
rs956572
BCL2
0.742 0.280 18 63153338 intron variant A/G snv 0.65 11
rs17070145
WWC1
0.790 0.120 5 168418786 intron variant C/T snv 0.43 10
rs3764650
ABCA7
0.790 0.200 19 1046521 intron variant T/G snv 0.14 9
rs17518584
CADM2
0.827 0.160 3 85555773 intron variant C/T snv 0.50 8
rs11931074
SNCA ; LOC105377329
0.851 0.080 4 89718364 intron variant G/A;C;T snv 7
rs223331
CISD2
0.851 0.160 4 102872408 intron variant T/A;C snv 5
rs2306604
TFAM
0.827 0.080 10 58388932 intron variant A/C;G;T snv 5
rs3764435
ALDH1A1
0.827 0.120 9 72901960 intron variant A/C;T snv 5
rs223330
CISD2
0.851 0.160 4 102872502 intron variant T/A;C snv 4
rs63751011
MAPT
0.925 0.120 17 46010418 intron variant C/T snv 4
rs9331896
CLU ; MIR6843
0.851 0.080 8 27610169 intron variant C/G;T snv 4
rs2235751
PDYN-AS1 ; PDYN
0.882 0.120 20 1989288 intron variant A/G snv 0.40 3
rs2420616
GRK5
0.882 0.080 10 119316984 intron variant A/G snv 0.69 3
rs2618516
SPON1
0.882 0.080 11 14000092 intron variant T/C snv 0.65 3
rs4752293
GRK5
0.882 0.080 10 119342186 intron variant C/T snv 0.74 3
rs6489630
NTF3
0.882 0.080 12 5495458 intron variant T/C snv 0.75 3
rs8126696 0.882 0.080 21 37358422 intron variant T/C snv 0.64 3
rs9397456
ESR1
0.882 0.160 6 151926017 intron variant A/G;T snv 3
rs1884049
ESR1
0.925 0.080 6 151966232 intron variant T/C snv 0.75 2
rs2337506
CHRNA7
0.925 0.080 15 32053864 intron variant A/G snv 0.60 2
rs8027814
CHRNA7
0.925 0.080 15 32058469 intron variant G/A snv 0.57 2