Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 10
rs929843
PDXDC2P ; PDXDC2P-NPIPB14P
16 70011845 non coding transcript exon variant A/C snv 0.84 1
rs6555855 5 169322733 intergenic variant G/A snv 0.83 1
rs7103411
BDNF ; BDNF-AS
0.752 0.160 11 27678578 intron variant C/T snv 0.82 15
rs865809
EEF1AKMT4-ECE2 ; ECE2
3 184279947 intron variant A/G snv 0.82 1
rs1618689
CAMK4
5 111270357 intron variant C/G snv 0.81 1
rs545075 11 94338512 intergenic variant G/C snv 0.81 1
rs1930170
PCDH15
10 54457992 intron variant A/G snv 0.80 1
rs939317
EIF4G1
3 184328011 intron variant A/C;G snv 0.76 0.80 1
rs7102513
FZD4-DT
11 87006945 intron variant T/C snv 0.80 1
rs2604264 9 74289671 intergenic variant C/G snv 0.79 1
rs9795476
SIRT3 ; PSMD13
11 235894 intron variant T/G snv 0.79 1
rs1038903 4 28750432 intergenic variant C/T snv 0.79 1
rs12656569 5 169311587 intergenic variant A/C snv 0.79 1
rs298088
PDE4D
5 59698700 intron variant A/G snv 0.79 1
rs6964833
GTF2I
7 74687575 intron variant C/T snv 0.78 1
rs7617480
KLHDC8B
3 49173299 intron variant A/C snv 0.76 1
rs480263
LOC105375951
9 1709382 regulatory region variant T/G snv 0.76 1
rs9849248 3 88192124 intergenic variant C/T snv 0.74 1
rs349356
KCNB2
8 72541711 intron variant G/T snv 0.74 1
rs338070 2 44948150 downstream gene variant C/G snv 0.73 1
rs3914188
EEF1AKMT4-ECE2 ; ECE2
3 184292260 3 prime UTR variant G/C snv 0.73 0.73 2
rs6575806
RTL1
14 100886874 intron variant C/A snv 0.72 1
rs395962
LIN28B
6 104949543 intron variant T/G snv 0.72 6
rs2391504
LINC02465
4 129809917 intron variant A/G snv 0.72 1