Disease: Schizophrenia
Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs105633
DELE1 ; PCDH12
0.882 0.040 5 141945684 synonymous variant T/C;G snv 0.98; 4.0E-06 3
rs11125080
ATP6V1E2
0.882 0.040 2 46505266 intron variant G/A;C snv 3
rs11829119
LOC107984527
0.851 0.040 12 19040597 intergenic variant T/A;C snv 4
rs12052005
CCDC102B
0.882 0.040 18 68832311 intron variant G/C;T snv 3
rs12443954 0.851 0.040 16 89675088 intron variant A/C;G snv 5
rs138449918
SLC8A1-AS1
0.882 0.040 2 39936810 intron variant AT/-;ATAT delins 3
rs141252918
CCDC170
0.882 0.040 6 151506923 intron variant G/A;C snv 4
rs142425863 0.925 0.040 6 29783976 intergenic variant C/T snv 2
rs144373461 0.925 0.040 6 29783228 intergenic variant C/A snv 2
rs1555454508
SPG11
0.790 0.240 15 44615487 stop gained GTA/ATC mnv 18
rs17154917 0.851 0.040 7 81207393 intergenic variant G/A;T snv 4
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 5
rs2054399
KCNMB2-AS1 ; KCNMB2
0.925 0.040 3 178623794 intron variant G/A;C snv 4
rs221774 0.851 0.080 7 100701361 upstream gene variant A/G;T snv 4
rs221798
GIGYF1
0.882 0.040 7 100689872 intron variant C/A;G snv 3
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 5
rs2721800
MPP6
0.851 0.040 7 24652933 intron variant G/A;C;T snv 5
rs312262717
SPG11
0.790 0.240 15 44659104 frameshift variant A/-;AA delins 18
rs6558872
CSMD1
0.882 0.040 8 4380617 intron variant G/A;C snv 3
rs7405404 0.925 0.040 16 13656002 intergenic variant T/A;C snv 3
rs7766730 0.882 0.040 6 65987110 intergenic variant C/A;T snv 3
rs7959663
MYO1H
0.925 0.040 12 109446562 intron variant G/A;C snv 2
rs9297357
ZFPM2 ; LOC105375695
0.851 0.040 8 105130105 intron variant C/G;T snv 5
rs9862857
LOC101927995 ; LOC105377013
0.851 0.040 3 30453840 regulatory region variant A/G;T snv 4
rs9951150 0.851 0.040 18 55153893 intergenic variant A/G;T snv 5