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
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs777919630
CBS
0.623 0.680 21 43062358 missense variant G/A;T snv 8.0E-06; 4.0E-06 40
rs75932628
LOC105375056 ; TREM2
0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs33939927
LRRK2
0.708 0.120 12 40310434 missense variant C/A;G;T snv 4.0E-06; 1.2E-05 24
rs63750231
PSEN1
0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs63750083
PSEN1
0.732 0.160 14 73219177 missense variant C/A;T snv 13
rs7895833 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 12
rs4717806
LOC105375350 ; STX1A ; BUD23
0.776 0.200 7 73702147 intron variant T/A;C snv 9
rs2298813
SORL1
0.790 0.120 11 121522975 missense variant G/A;T snv 7.2E-02; 4.0E-06 7
rs104894103
APTX
0.807 0.280 9 32974495 stop gained C/G;T snv 4.0E-06; 1.6E-04 6
rs7354779
DNMT3L ; DNMT3L-AS1
0.827 0.200 21 44250887 missense variant T/C snv 0.21 6
rs12344615
UBQLN1
0.851 0.080 9 83666280 intron variant A/C;G snv 4
rs59007384
TOMM40
0.851 0.080 19 44893408 intron variant G/A;T snv 4
rs5978930
ANOS1
0.882 0.080 X 8642266 intron variant T/C;G snv 4
rs9357347
LOC107986595
0.851 0.080 6 41182853 intergenic variant A/C;T snv 4
rs1859788
PILRA
0.925 0.080 7 100374211 missense variant A/C;G snv 4.0E-06; 0.65 3
rs1451603364
BDNF-AS ; BDNF
0.925 0.120 11 27658411 missense variant C/T snv 4.0E-06 2
rs4837766
CDK5RAP2
0.925 0.080 9 120402006 intron variant A/C;G;T snv 2
rs4978818
PALM2AKAP2 ; PTPN3
0.925 0.120 9 109509949 intron variant G/A;C;T snv 2
rs528528
RELN
0.925 0.080 7 103748638 intron variant T/A;C snv 2
rs63750048
PSEN2
0.925 0.080 1 226883817 missense variant C/T snv 4.0E-06 2
rs1130399
HLA-DQB1
1.000 0.040 6 32661978 missense variant G/A;T snv 0.20 1
rs1334496 1.000 0.040 X 137178554 intergenic variant C/A;T snv 1
rs227959 1.000 0.040 17 3406923 upstream gene variant C/T snv 1