Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs4906902
GABRB3
0.724 0.200 15 26774621 intron variant A/G snv 0.15 14
rs4523957
SMG6 ; SRR
0.790 0.120 17 2305605 intron variant G/T snv 0.54 9
rs10868235
NTRK2
0.925 0.040 9 84878840 intron variant C/T snv 0.40 6
rs1867283
NTRK2
0.925 0.080 9 84835851 intron variant G/A snv 0.39 5
rs844347
ASIC1
1.000 0.040 12 50067893 intron variant A/C snv 0.32 1
rs944688
GABBR2
1.000 0.040 9 98601678 intron variant C/T snv 0.35 1
rs35753505 0.827 0.080 8 31616625 intergenic variant T/A;C snv 6
rs2020918 0.925 0.080 8 42214920 intergenic variant A/G snv 0.71 2
rs61738009
CPA6 ; LOC102724708
0.827 0.080 8 67483807 stop gained C/A;T snv 4.0E-06; 2.0E-03 2.5E-03 11
rs104894718
SCN1B
0.790 0.160 19 35033654 stop gained C/A;G;T snv 4.0E-06 8
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
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1801278
IRS1
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs1799990
PRNP
0.683 0.440 20 4699605 missense variant A/G snv 0.31 0.33 23
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs1805097
IRS2
0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 22
rs2986017
CALHM1
0.851 0.120 10 103458495 missense variant A/G snv 0.79 0.80 6
rs118192250
KCNQ3
0.851 0.120 8 132175457 missense variant C/A snv 5
rs16990018
PRNP
0.882 0.120 20 4699732 missense variant A/G snv 3.8E-03 1.6E-02 5
rs1057517661
LOC107984343 ; GAL
0.925 0.040 11 68685628 missense variant C/A;T snv 2
rs137852779
EFHC1
1.000 0.040 6 52438538 missense variant A/G snv 4.0E-06 2
rs1398830127
GABBR1
0.925 0.080 6 29610981 missense variant C/T snv 4.1E-06 2
rs1805057
GABBR1
0.925 0.080 6 29613344 missense variant C/T snv 1.1E-03 1.5E-03 2