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
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35 16
rs2070951
NR3C2
0.776 0.320 4 148436862 splice region variant G/A;C snv 4.2E-06; 0.53 9
rs879255273
CCN6
0.925 0.040 6 112064998 splice donor variant G/A snv 7
rs174575
FADS2
1.000 0.040 11 61834531 intron variant C/G snv 0.25 3
rs781986930
CCN6
1.000 0.040 6 112069565 missense variant G/A;C snv 4.0E-06; 4.0E-06 2
rs1480620991
COL2A1
0.925 0.040 12 47984580 missense variant C/G snv 4.0E-06 2
rs869312907
COL2A1
0.925 0.040 12 47995910 missense variant C/T snv 2
rs174553
FADS1 ; FADS2
1.000 0.040 11 61807686 intron variant A/G;T snv 0.28 2
rs121908899
CCN6
1.000 0.040 6 112064842 missense variant G/A;C snv 1
rs121908900
CCN6
1.000 0.040 6 112069548 stop gained G/A snv 4.0E-06 1
rs121908901
CCN6
1.000 0.040 6 112061098 stop gained C/A;T snv 4.0E-05; 4.0E-06 2.1E-05 1
rs121908902
CCN6
1.000 0.040 6 112061174 missense variant T/C snv 1
rs121908903
CCN6
1.000 0.040 6 112069555 missense variant T/C snv 1
rs1562595388
CCN6
1.000 0.040 6 112061175 missense variant G/A snv 1
rs1562599153
CCN6
1.000 0.040 6 112068307 frameshift variant T/- del 1
rs727503755
CCN6
1.000 0.040 6 112068352 frameshift variant GT/- delins 8.0E-06 7.0E-06 1
rs781838640
CCN6
1.000 0.040 6 112069421 frameshift variant AG/- delins 1
rs782172825
CCN6
1.000 0.040 6 112061139 missense variant G/A snv 2.1E-05 1
rs782813346
CCN6
1.000 0.040 6 112068282 missense variant T/C;G snv 1.2E-05 7.0E-06 1
rs797044438
CCN6
1.000 0.040 6 112061188 frameshift variant A/- del 1
rs797044439
CCN6
1.000 0.040 6 112054406 splice donor variant -/T delins 1