Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs12273363
BDNF
0.807 0.120 11 27723312 intron variant T/C snv 0.16 11
rs7127507
BDNF-AS ; BDNF
0.827 0.080 11 27693337 intron variant T/C snv 0.34 6
rs1977412
LOC105373166
0.882 0.160 1 230716523 intron variant T/A;C snv 5
rs2732260
FUT10
0.882 0.200 8 33431749 intron variant G/A snv 8.4E-02 5
rs8074995
PRKCA
0.925 0.040 17 66796013 intron variant G/A snv 0.13 5
rs63751011
MAPT
0.925 0.120 17 46010418 intron variant C/T snv 4
rs1411832
LOC105378469
1.000 0.040 10 106126497 intergenic variant C/T snv 0.10 2
rs104894396
GJB2
0.672 0.400 13 20189511 stop gained C/T snv 5.8E-04 1.1E-04 28
rs555145190
NAGLU
0.732 0.360 17 42543921 stop gained G/A;C;T snv 4.2E-06 21
rs713041
GPX4
0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 16
rs763868966
GFAP
1.000 0.080 17 44911429 stop gained C/A;G;T snv 1.2E-05; 4.0E-05 4
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 42
rs28937900
FKRP
0.752 0.160 19 46756276 missense variant C/A;T snv 1.0E-03 37
rs370717845
HGSNAT
0.763 0.320 8 43161462 missense variant G/A snv 33
rs63750424
MAPT
0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30
rs148881970
NAGLU
0.724 0.360 17 42543840 missense variant A/G snv 5.4E-05 1.3E-04 22
rs781049584
APP
0.724 0.280 21 26021917 missense variant T/G snv 8.2E-06 7.0E-06 18
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 17
rs74315408
PRNP
0.752 0.280 20 4699758 missense variant G/A snv 6.4E-05 4.2E-05 16