Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs6311
HTR2A
0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs9357271
BTBD9
0.776 0.160 6 38398097 intron variant T/C snv 0.38 8
rs1805502
GRIN2B
0.790 0.200 12 13561247 3 prime UTR variant A/G snv 0.25 7
rs518147
HTR2C
0.807 0.200 X 114584109 5 prime UTR variant C/A;G snv 7
rs25532
LOC105371720 ; SLC6A4
0.851 0.160 17 30237152 upstream gene variant G/A snv 6.3E-02 5
rs3813929
HTR2C
0.851 0.240 X 114584047 upstream gene variant C/G;T snv 5
rs1805476
GRIN2B
0.851 0.160 12 13561429 3 prime UTR variant G/T snv 0.33 4
rs1906252 0.925 0.120 6 98102413 intron variant C/A;T snv 3
rs9296249
BTBD9
0.882 0.120 6 38398065 intron variant T/C snv 0.30 3
rs11149058
LOC105370269
0.925 0.120 13 76978136 downstream gene variant T/A;C;G snv 2
rs193302861
SLITRK1
0.925 0.120 13 83880244 frameshift variant G/- delins 2
rs4271390
NECTIN1
0.925 0.120 11 119655426 intron variant T/C snv 0.68 2
rs4714156
BTBD9
0.925 0.120 6 38393336 intron variant C/T snv 0.36 2
rs4988462
POU1F1
0.925 0.120 3 87264203 intron variant C/T snv 0.31 2
rs10846381
LMO3 ; MGST1
1.000 0.120 12 16599165 non coding transcript exon variant A/T snv 0.46 1
rs11264126
DLGAP3
1.000 0.120 1 34876494 intron variant G/A snv 0.41 1
rs11603305 1.000 0.120 11 10976402 regulatory region variant A/G snv 0.28 1
rs117648881
CSMD3
1.000 0.120 8 112569669 intron variant G/A snv 1.6E-02 1
rs12141243
DLGAP3
1.000 0.120 1 34881321 intron variant T/C snv 9.7E-02 1
rs12459560
ZNF577 ; FPR3
1.000 0.120 19 51815127 intron variant G/T snv 0.14 1
rs13407215 1.000 0.120 2 160688380 intergenic variant C/T snv 4.3E-02 1
rs150975336
MUC16
1.000 0.120 19 8995481 intergenic variant C/G snv 2.7E-02 1
rs191044310 1.000 0.120 10 23416522 intergenic variant T/A snv 1.3E-02 1