Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2841307 6 100308811 intergenic variant C/T snv 0.20 2
rs4996815 13 105999312 intron variant G/T snv 0.61 2
rs6589386 1.000 0.040 11 113573031 intergenic variant C/T snv 0.36 2
rs6627057 X 145059799 downstream gene variant T/G snv 0.16 2
rs6913660 1.000 0.040 6 27123646 upstream gene variant C/A snv 0.14 2
rs6932590 1.000 0.040 6 27281152 downstream gene variant T/C snv 0.26 2
rs7727102 5 4720472 intron variant G/C snv 0.32 2
rs7912580 1.000 0.040 10 62156213 regulatory region variant G/A snv 7.6E-02 2
rs2789588 6 72433995 intergenic variant A/C snv 0.26 1
rs11740562
ADAM19
5 157515277 intron variant A/G snv 7.1E-02 2
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs3730358
AKT1
0.724 0.360 14 104780070 intron variant G/A;C snv 0.16; 4.0E-03 14
rs1130214
AKT1
0.742 0.280 14 104793397 5 prime UTR variant C/A snv 0.31 12
rs2494732
AKT1
0.763 0.240 14 104772855 intron variant T/C snv 0.50 0.47 11
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs10994359
ANK3
0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 7
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs893924483
BDNF ; BDNF-AS
0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 23
rs6024905
BPI
20 38329435 intron variant G/A snv 0.47 2
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs2007044
CACNA1C
0.882 0.040 12 2235794 intron variant A/G snv 0.50 6
rs4765905
CACNA1C
0.827 0.040 12 2240418 intron variant G/A;C snv 6