Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs242924
LINC02210-CRHR1 ; MAPT-AS1 ; CRHR1
0.882 0.080 17 45808001 intron variant G/T snv 0.44 3
rs2910931
MIR579 ; ZFR
0.925 0.080 5 32394809 intron variant T/A snv 0.63 3
rs10216809
SGCZ
0.925 0.080 8 14507414 intron variant C/G;T snv 2
rs10894993 0.925 0.080 11 100627998 intergenic variant T/G snv 4.7E-02 2
rs11179000
TPH2
0.925 0.040 12 71944848 intron variant A/T snv 0.31 2
rs11210604 0.925 0.080 1 42158001 downstream gene variant T/A;G snv 2
rs11724320
NPY5R ; NPY1R
0.925 0.040 4 163346771 intron variant T/C snv 0.56 2
rs17035816
GLRB
0.925 0.040 4 157167312 intron variant A/G snv 0.11 2
rs1799923
CCK
0.925 0.040 3 42264802 5 prime UTR variant A/G snv 0.82 2
rs4076452
LINC02210-CRHR1
1.000 0.040 17 45778528 intron variant G/C snv 0.16 2
rs4760820
TPH2
0.925 0.040 12 72003216 intron variant C/G snv 0.29 2
rs7688285 0.925 0.040 4 157047466 intergenic variant G/A snv 0.10 2
rs10415555
PEPD
1.000 0.040 19 33519283 intron variant A/G snv 0.19 1
rs10454453
PDE4B
1.000 0.040 1 66206849 intron variant C/A snv 0.48 1
rs10801152
LOC105371665
1.000 0.040 1 192792174 intron variant A/T snv 0.31 1
rs10875995
ASIC1
1.000 0.040 12 50068355 intron variant T/A;C snv 1
rs10879357
TPH2
1.000 0.040 12 72020783 intron variant A/G snv 0.59 1
rs11060369
TMEM132D
1.000 0.040 12 129475652 intron variant A/C snv 0.41 1
rs11763020
C7orf50
1.000 0.040 7 1020652 intron variant C/T snv 0.12 1
rs11805657
RGS7
1.000 0.040 1 240955726 intron variant T/C snv 0.87 1
rs12061304
LOC107985174
1.000 0.040 1 110695063 intergenic variant A/G snv 0.30 1
rs13356494 1.000 0.040 5 135991866 regulatory region variant C/G;T snv 1
rs1418688 1.000 0.040 6 71169166 downstream gene variant A/G;T snv 1
rs144783209
SMAD1
1.000 0.040 4 145482377 intron variant G/C;T snv 1
rs1487275
TPH2
1.000 0.040 12 72016512 intron variant C/A snv 0.71 1