Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10216809
SGCZ
0.925 0.080 8 14507414 intron variant C/G;T snv 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
rs1050450
GPX1
0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs10801152
LOC105371665
1.000 0.040 1 192792174 intron variant A/T snv 0.31 1
rs10801153 0.925 0.080 1 192794818 intron variant G/A snv 0.27 3
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
rs10894993 0.925 0.080 11 100627998 intergenic variant T/G snv 4.7E-02 2
rs11030104
BDNF ; BDNF-AS
0.790 0.240 11 27662970 intron variant A/G snv 0.16 12
rs11060369
TMEM132D
1.000 0.040 12 129475652 intron variant A/C snv 0.41 1
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
rs1133503
MANEA
1.000 0.040 6 95606712 3 prime UTR variant C/G;T snv 4
rs11724320
NPY5R ; NPY1R
0.925 0.040 4 163346771 intron variant T/C snv 0.56 2
rs1173546708
TPH1
0.851 0.120 11 18040661 synonymous variant G/A snv 4.0E-06 5
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
rs11946004
NPY5R
0.925 0.040 4 163351551 synonymous variant G/A;T snv 0.10; 4.0E-06 2
rs12061304
LOC107985174
1.000 0.040 1 110695063 intergenic variant A/G snv 0.30 1
rs1245554802
CAMK1 ; OGG1
0.851 0.120 3 9765892 splice acceptor variant T/C snv 4.0E-06 5
rs12579350
ANO2
0.882 0.080 12 5687935 intron variant G/A snv 0.12 3
rs1326656542
LIG4
0.776 0.280 13 108210293 missense variant A/T snv 4.0E-06 10
rs13356494 1.000 0.040 5 135991866 regulatory region variant C/G;T snv 1