Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1256030
ESR2
0.827 0.240 14 64280452 intron variant A/G;T snv 6
rs3818361
CR1
0.851 0.080 1 207611623 intron variant A/G snv 0.74 6
rs6584400
NRG3
0.851 0.120 10 81896770 intron variant G/A snv 0.22 6
rs17746510
RAPGEF4
0.882 0.080 2 173019562 intron variant T/C;G snv 5
rs3764435
ALDH1A1
0.827 0.120 9 72901960 intron variant A/C;T snv 5
rs8074995
PRKCA
0.925 0.040 17 66796013 intron variant G/A snv 0.13 5
rs9951307
AQP4-AS1
0.882 0.120 18 26850565 intron variant G/A snv 0.65 5
rs11637611
PARP6
0.851 0.160 15 72259371 intron variant C/T snv 0.63 4
rs11887120
DNMT3A
0.882 0.080 2 25262866 intron variant C/T snv 0.45 4
rs16947151
ABI3
0.882 0.080 17 49213276 intron variant A/G snv 0.12 4
rs5978930
ANOS1
0.882 0.080 X 8642266 intron variant T/C;G snv 4
rs7840202
UBR5
0.851 0.160 8 102296172 intron variant A/C snv 0.21 4
rs11030108
BDNF ; BDNF-AS
1.000 0.040 11 27673917 intron variant A/G snv 0.72 3
rs1938526
ANK3
0.882 0.040 10 60540625 intron variant A/G snv 8.3E-02 3
rs2189814
GRM3
0.925 0.040 7 86702440 intron variant T/A;C snv 3
rs3763040
AQP4 ; AQP4-AS1
0.925 0.080 18 26864410 intron variant G/A;T snv 3
rs3875089
AQP4 ; AQP4-AS1
0.925 0.080 18 26865469 intron variant T/C snv 0.19 3
rs55781031
BCHE
0.925 0.080 3 165786432 intron variant A/G snv 5.3E-02 3
rs62256378
SUCLG2
0.925 0.080 3 67406609 intron variant G/A;C snv 3
rs6910730
TREM1
0.925 0.080 6 41278895 intron variant A/G snv 0.21 3
rs10521467
PCSK5
0.925 0.080 9 76036575 intron variant A/G snv 0.12 2
rs1157659 1.000 0.040 11 27736075 intron variant A/G snv 0.37 2
rs115881343
TOMM40
1.000 0.040 19 44899959 intron variant C/G;T snv 2.9E-02 2
rs13333659
CBFA2T3
1.000 0.040 16 88972472 intron variant G/T snv 0.13 2
rs17601241
MIR4713HG ; CYP19A1
1.000 0.040 15 51215677 intron variant G/A snv 0.11 8.6E-02 2