Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs5848
FAM171A2 ; GRN
0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 17
rs1990622 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 16
rs3812718
SCN1A-AS1 ; SCN1A
0.776 0.240 2 166053034 splice region variant C/T snv 0.48 8
rs104894718
SCN1B
0.790 0.160 19 35033654 stop gained C/A;G;T snv 4.0E-06 8
rs704180
ABCC9
0.807 0.240 12 21841177 intron variant A/G snv 0.55 6
rs73069071
IAPP ; SLCO1A2
0.807 0.240 12 21357370 intron variant T/C snv 0.14 6
rs16990018
PRNP
0.882 0.120 20 4699732 missense variant A/G snv 3.8E-03 1.6E-02 5
rs527479125
DEPDC5
1.000 22 31845200 missense variant G/A;T snv 8.0E-06 1
rs748813142
DEPDC5
1.000 22 31754941 missense variant A/G snv 6.0E-05 7.0E-06 1
rs754059546
DEPDC5
1.000 22 31845227 missense variant G/A snv 1.2E-05 1