Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10894993 0.925 0.080 11 100627998 intergenic variant T/G snv 4.7E-02 2
rs1386494
TPH2
0.790 0.120 12 71958763 intron variant T/C;G snv 0.82 7
rs6502892
MIR22 ; MIR22HG
1.000 0.040 17 1714314 intron variant T/C;G snv 1
rs5751876
ADORA2A ; ADORA2A-AS1 ; SPECC1L-ADORA2A
0.742 0.320 22 24441333 synonymous variant T/C snv 0.54 0.52 16
rs3213207
DTNBP1
0.776 0.120 6 15627871 intron variant T/C snv 8.7E-02 11
rs1386483
TPH2
0.790 0.080 12 72018714 intron variant T/C snv 0.53 9
rs1245554802
CAMK1 ; OGG1
0.851 0.120 3 9765892 splice acceptor variant T/C snv 4.0E-06 5
rs945032
BDKRB2
0.882 0.040 14 96204324 upstream gene variant T/C snv 0.78 5
rs11724320
NPY5R ; NPY1R
0.925 0.040 4 163346771 intron variant T/C snv 0.56 2
rs11805657
RGS7
1.000 0.040 1 240955726 intron variant T/C snv 0.87 1
rs4448731 1.000 0.040 12 71935326 upstream gene variant T/C snv 0.40 1
rs7309727
TMEM132D
1.000 0.040 12 129470814 intron variant T/C snv 0.75 1
rs7788
SNAPC2
1.000 0.040 19 7923232 3 prime UTR variant T/C snv 0.28 1
rs4746
GLO1
0.708 0.400 6 38682852 missense variant T/A;G snv 0.36 21
rs11210604 0.925 0.080 1 42158001 downstream gene variant T/A;G snv 2
rs10875995
ASIC1
1.000 0.040 12 50068355 intron variant T/A;C snv 1
rs1819741 1.000 0.040 1 192815708 intron variant T/A;C snv 1
rs4684677
GHRLOS ; GHRL
0.742 0.360 3 10286769 missense variant T/A snv 0.10 6.6E-02 13
rs2910931
MIR579 ; ZFR
0.925 0.080 5 32394809 intron variant T/A snv 0.63 3
rs9372078 1.000 0.040 6 150592825 intergenic variant T/A snv 0.73 1
rs4570625
TPH2
0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs1800532
TPH1
0.763 0.160 11 18026269 intron variant G/T snv 0.33 15
rs242924
LINC02210-CRHR1 ; MAPT-AS1 ; CRHR1
0.882 0.080 17 45808001 intron variant G/T snv 0.44 3
rs144783209
SMAD1
1.000 0.040 4 145482377 intron variant G/C;T snv 1
rs4076452
LINC02210-CRHR1
1.000 0.040 17 45778528 intron variant G/C snv 0.16 2