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
rs1801198
TCN2
0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 26
rs769236847
CZ1P-ASNS ; ASNS
0.807 0.200 7 97869011 missense variant C/T snv 4.0E-06 3.5E-05 8
rs870142
STX18-AS1
0.851 0.120 4 4646320 intron variant C/G;T snv 7
rs16835979
STX18-AS1
0.851 0.120 4 4633549 intron variant C/A snv 0.20 6
rs6824295
STX18-AS1
0.851 0.120 4 4612553 intron variant C/T snv 0.20 6
rs779545541
GPHN
0.882 0.120 14 66965293 missense variant C/T snv 4.0E-06 5
rs141441277
SYTL4
0.882 0.120 X 100689933 missense variant G/A snv 5.6E-04 3.8E-04 5
rs1800692
TNFRSF1A
0.925 0.120 12 6333180 missense variant A/G snv 0.64 0.71 5
rs1340513
KDM4C
0.882 0.120 9 6977633 intron variant G/A snv 0.75 4
rs762292772
SHANK3
0.882 0.160 22 50721505 frameshift variant G/-;GG delins 4
rs1555226315
TBX5
0.925 0.120 12 114398639 stop gained C/T snv 4
rs769402060
CYP1B1-AS1 ; CYP1B1
0.925 0.120 2 38075022 missense variant A/G snv 3.3E-05 4.2E-05 3
rs2298444
FOLR2
0.925 0.120 11 72221370 intron variant T/C snv 0.27 3
rs1114167356
TPM1
1.000 0.080 15 63062261 missense variant C/T snv 1