Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4341581
TPH2
1.000 0.040 12 71941293 intron variant G/T snv 0.97 1
rs6537825
TRIM33
1.000 0.040 1 114405659 missense variant A/G snv 0.88 0.92 1
rs4773054 1.000 0.040 13 109501681 intron variant T/C snv 0.89 2
rs288604 1.000 0.040 16 62638708 intergenic variant G/A snv 0.87 1
rs1409313
CUEDC2
1.000 0.040 10 102431844 intron variant T/C snv 0.85 2
rs10732392
LMX1B
1.000 0.040 9 126633758 intron variant A/G snv 0.84 1
rs1936295 1.000 0.040 10 117902581 intergenic variant T/C snv 0.83 1
rs25925
CAMK4
0.925 0.040 5 111484055 synonymous variant G/C snv 0.75 0.83 2
rs7834018 1.000 0.040 8 71649507 intergenic variant C/T snv 0.83 1
rs2292813
SLC25A12
0.882 0.040 2 171787719 intron variant T/C snv 0.81 3
rs2150291
SYNE2
1.000 0.040 14 63864705 intron variant T/C snv 0.81 1
rs6537835 1.000 0.040 1 114566293 downstream gene variant G/A snv 0.80 1
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs2056202
SLC25A12
0.882 0.040 2 171855970 intron variant T/C snv 0.81 0.77 4
rs1340513
KDM4C
0.882 0.120 9 6977633 intron variant G/A snv 0.75 4
rs29456 1.000 0.040 5 66244019 intergenic variant T/C snv 0.73 1
rs1861973
EN2
0.925 0.040 7 155461450 intron variant T/C snv 0.73 2
rs1861972
EN2
0.925 0.040 7 155461298 intron variant G/A snv 0.72 2
rs7925879
ROBO3
1.000 0.040 11 124870795 intron variant A/G snv 0.72 1
rs3923890
ROBO3
1.000 0.040 11 124870514 intron variant A/T snv 0.72 1
rs4701259 1.000 0.040 5 25900989 intergenic variant A/G snv 0.71 1
rs4701511 1.000 0.040 5 25895895 intergenic variant C/A snv 0.71 1
rs7705715 1.000 0.040 5 25899305 intergenic variant T/C snv 0.71 1
rs237889
CAV3 ; OXTR
0.925 0.040 3 8760797 intron variant T/C snv 0.71 2
rs6590109
ROBO4
1.000 0.040 11 124889152 intron variant G/A snv 0.70 1