Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6277
DRD2
0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs370717845
HGSNAT
0.763 0.320 8 43161462 missense variant G/A snv 33
rs1555735545
STRN4 ; FKRP
0.851 0.160 19 46746071 5 prime UTR variant G/A snv 22
rs74315408
PRNP
0.752 0.280 20 4699758 missense variant G/A snv 6.4E-05 4.2E-05 16
rs80356702
CLCN1
0.882 0.120 7 143330868 missense variant G/A snv 4.0E-06 1.4E-05 9
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
rs781587642
TUBA4A ; STK16
0.851 0.120 2 219250557 missense variant G/A;C snv 2.0E-05 6
rs555145190
NAGLU
0.732 0.360 17 42543921 stop gained G/A;C;T snv 4.2E-06 21
rs775129479
SPSB3 ; IGFALS
0.851 0.120 16 1791387 missense variant G/A;C;T snv 1.6E-05; 8.1E-06; 8.1E-06 6
rs63750852
PSEN1
0.790 0.120 14 73170998 missense variant G/A;T snv 8
rs1352010373
TMEM94
0.641 0.560 17 75489265 splice acceptor variant G/C snv 73
rs768823392
SPG7
0.827 0.120 16 89546657 coding sequence variant GGCGGGAGA/- delins 2.6E-04 4.2E-04 10
rs713041
GPX4
0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 16
rs1977412
LOC105373166
0.882 0.160 1 230716523 intron variant T/A;C snv 5
rs572842823
APP
0.763 0.160 21 25897626 missense variant T/A;G snv 11
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
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
rs61748411
MECP2
0.925 0.120 X 154031356 missense variant T/C snv 3
rs536551654
NGFR ; LOC100288866
1.000 0.120 17 49511972 missense variant T/C snv 2
rs781049584
APP
0.724 0.280 21 26021917 missense variant T/G snv 8.2E-06 7.0E-06 18