Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs210152
GGNBP1
1.000 0.040 6 33547743 intron variant G/A snv 0.86 1
rs1198589 1.000 0.040 1 98084855 intergenic variant T/C snv 0.85 1
rs4968678
SCN4A ; LOC105371858
1.000 0.040 17 63966848 intron variant A/G snv 0.85 1
rs7713886
HTR4
1.000 0.040 5 148645595 non coding transcript exon variant C/T snv 0.85 1
rs4234898 1.000 0.040 4 156077389 intergenic variant T/C snv 0.85 2
rs10744422
HIP1R
1.000 0.040 12 122852242 intron variant T/C snv 0.85 1
rs1734907 0.925 0.080 7 100717894 upstream gene variant A/G snv 0.84 4
rs2270954
DCC ; LINC01917
1.000 0.040 18 53530928 3 prime UTR variant A/C snv 0.84 1
rs1548359
CDC45
1.000 0.040 22 19515751 intron variant G/C snv 0.84 1
rs6785
CREB1 ; METTL21A
0.851 0.120 2 207603273 3 prime UTR variant A/G snv 0.84 4
rs2868985
LOC105374690 ; MIR217HG
1.000 0.040 2 55964335 intron variant G/A snv 0.84 1
rs281768
MAIP1
1.000 0.040 2 199960517 intron variant A/T snv 0.84 2
rs2745557
PACERR ; PTGS2
0.807 0.200 1 186680089 intron variant A/G snv 0.83 6
rs6502097
SECTM1
0.882 0.040 17 82328303 5 prime UTR variant C/G snv 0.83 3
rs7319102
PCDH17
1.000 0.040 13 57678667 intron variant G/A snv 0.83 3
rs2144683
LOC101928354
1.000 0.040 6 14717284 intron variant C/G snv 0.83 2
rs548181
FEZ1 ; STT3A-AS1 ; STT3A
0.851 0.040 11 125591814 5 prime UTR variant A/G snv 0.83 5
rs3845702
CWC22
1.000 0.040 2 179983761 intron variant C/A snv 0.83 1
rs988748
BDNF
0.882 0.120 11 27703198 intron variant C/G snv 0.83 3
rs2660304
MIR137HG ; MIR137 ; MIR2682
0.925 0.120 1 98046571 non coding transcript exon variant G/T snv 0.83 2
rs7550768 1.000 0.040 1 11620226 upstream gene variant C/T snv 0.82 1
rs1191551 1.000 0.040 14 29531199 intergenic variant T/G snv 0.82 1
rs7103411
BDNF ; BDNF-AS
0.752 0.160 11 27678578 intron variant C/T snv 0.82 15
rs1902666
GRID1
1.000 0.040 10 86252022 intron variant C/T snv 0.82 1
rs2814351
GRID1
1.000 0.040 10 86249143 intron variant C/T snv 0.82 1