Disease: Schizophrenia
Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 5
rs1715
ZNF615
0.851 0.040 19 51991525 3 prime UTR variant T/C snv 1.4E-05 5
rs17662626
LOC107985969
0.851 0.040 2 193119895 intergenic variant A/G snv 5.9E-02 5
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 5
rs2021722
TRIM26
0.851 0.040 6 30206354 intron variant C/A;T snv 0.24 5
rs2524005
HLA-A
0.882 0.160 6 29931900 upstream gene variant G/A snv 0.18 5
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
rs2799573
CACNB2
0.851 0.040 10 18312999 intron variant T/C snv 0.20 5
rs3132581
MUCL3 ; HCG21 ; SFTA2
0.851 0.040 6 30945681 intron variant G/A snv 9.3E-02 5
rs548181
FEZ1 ; STT3A-AS1 ; STT3A
0.851 0.040 11 125591814 5 prime UTR variant A/G snv 0.83 5
rs6694545 0.851 0.040 1 29964421 intergenic variant A/G snv 0.58 5
rs7004633
LOC105375630
0.851 0.040 8 88748082 intron variant A/G snv 0.28 5
rs7914558
CNNM2
0.851 0.040 10 103016151 intron variant G/A snv 0.40 5
rs9297357
ZFPM2 ; LOC105375695
0.851 0.040 8 105130105 intron variant C/G;T snv 5
rs9834970 0.790 0.080 3 36814539 downstream gene variant T/C snv 0.45 5
rs9951150 0.851 0.040 18 55153893 intergenic variant A/G;T snv 5
rs10405744
ZNF93
0.851 0.040 19 19948684 intron variant G/A snv 9.0E-02 4
rs1054442
DDN
0.925 0.040 12 48995537 3 prime UTR variant A/C snv 0.46 4
rs10968749
LINGO2
0.851 0.040 9 28752486 intergenic variant A/G snv 5.5E-02 4
rs11004733
PCDH15
0.882 0.040 10 55089584 intron variant C/T snv 2.9E-02 4
rs11829119
LOC107984527
0.851 0.040 12 19040597 intergenic variant T/A;C snv 4
rs141252918
CCDC170
0.882 0.040 6 151506923 intron variant G/A;C snv 4
rs149268645
WDR12 ; CARF
0.882 0.040 2 202968295 intron variant G/A snv 8.4E-02 4
rs16875288
ADAMTS16 ; LOC101929200
0.851 0.040 5 5297087 intron variant A/T snv 0.22 4