Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs866294686
TRIM8 ; LOC105378460
0.683 0.480 10 102657073 stop gained C/A;T snv 43
rs1057524157
DEAF1
0.776 0.200 11 686962 missense variant A/C;T snv 19
rs1014959895
PRMT7
0.763 0.360 16 68329105 stop gained G/C;T snv 4.0E-06; 1.6E-05 16
rs1251713297
PRMT7
0.776 0.360 16 68355785 stop gained C/A snv 8.1E-06 15
rs1554944271
DEAF1
0.851 0.240 11 686925 missense variant C/G snv 14
rs1555103652
GRIN2B
0.882 0.240 12 13569973 missense variant A/C snv 11
rs757059851
LOC105377864 ; HTR1B
6 77462625 missense variant G/T snv 4.0E-06 1