Disease: Schizophrenia
Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 7
rs10275045
MAD1L1
0.882 0.160 7 1881190 intron variant C/T snv 0.35 5
rs10405744
ZNF93
0.851 0.040 19 19948684 intron variant G/A snv 9.0E-02 4
rs10503253
CSMD1
0.851 0.040 8 4323322 intron variant C/A snv 0.18 5
rs1054442
DDN
0.925 0.040 12 48995537 3 prime UTR variant A/C snv 0.46 4
rs105633
DELE1 ; PCDH12
0.882 0.040 5 141945684 synonymous variant T/C;G snv 0.98; 4.0E-06 3
rs10774037
CACNA1C
0.882 0.040 12 2311360 intron variant G/A snv 0.77 3
rs10968749
LINGO2
0.851 0.040 9 28752486 intergenic variant A/G snv 5.5E-02 4
rs10994359
ANK3
0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 5
rs10994397
ANK3
0.851 0.040 10 60519366 intron variant C/T snv 9.5E-02 5
rs11004733
PCDH15
0.882 0.040 10 55089584 intron variant C/T snv 2.9E-02 4
rs11125080
ATP6V1E2
0.882 0.040 2 46505266 intron variant G/A;C snv 3
rs11152369
TCF4
0.851 0.040 18 55399097 intron variant A/C snv 6.3E-02 5
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 5
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 12
rs115777110
LOC107985255
0.882 0.040 1 208936211 intergenic variant T/C snv 1.2E-02 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
rs12325410
LOC101927026
0.851 0.040 16 9581389 intron variant T/G snv 0.16 5
rs12443954 0.851 0.040 16 89675088 intron variant A/C;G snv 5
rs12576775
TENM4
0.827 0.080 11 79366149 intron variant A/G snv 0.15 6
rs12871532 0.851 0.040 13 108016199 intergenic variant T/C snv 0.46 5
rs12966547
LOC105372125
0.827 0.040 18 55084786 intergenic variant G/A snv 0.39 5
rs13001243 0.882 0.040 2 234306004 regulatory region variant G/A snv 7.5E-02 3
rs13072940 0.851 0.040 3 36801132 regulatory region variant T/A snv 0.37 5