Disease: Schizophrenia
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 13
rs10423928
GIPR
0.807 0.200 19 45679046 intron variant T/A snv 0.19 12
rs17514846
FURIN
0.882 0.120 15 90873320 intron variant C/A;G snv 7
rs6271
DBH-AS1 ; DBH
1.000 0.040 9 133657152 missense variant C/T snv 4.6E-02 4.8E-02 5
rs4129585
TSNARE1 ; LOC107986983
1.000 0.040 8 142231572 intron variant A/C snv 0.68 4
rs6740584
CREB1
0.882 0.040 2 207564627 intron variant T/C snv 0.37 4
rs12561919
C1orf167 ; C1orf167-AS1
1.000 0.040 1 11779866 missense variant C/T snv 0.13 0.13 3