Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4396807
TRIOBP
22 37742372 intron variant G/C snv 0.38 3
rs9616914
SHANK3
1.000 0.040 22 50678709 intron variant G/A snv 0.35 0.36 3
rs11090045
ZC3H7B
1.000 0.040 22 41357599 3 prime UTR variant G/A;C snv 2
rs2743461
CYP2D7
22 42144550 5 prime UTR variant G/A snv 0.60 2
rs28741121
XRCC6
22 41629819 intron variant G/A snv 0.11 2
rs5757673 22 39441915 downstream gene variant T/C snv 0.79 2
rs6518724 22 31008409 intergenic variant C/G;T snv 2
rs112367533
DGCR8
22 20104310 intron variant G/A;C snv 1
rs112699334
DEPDC5
22 31855624 intron variant T/C snv 2.2E-02 1
rs11703813
CCDC134
22 41814593 intron variant C/G;T snv 1
rs11704277
KCNJ4 ; LOC101927183
22 38430794 intron variant C/T snv 7.8E-02 1
rs117269860
SLC25A17
22 40790485 intron variant A/C snv 2.1E-02 1
rs12627753
EFCAB6
22 43597992 intron variant G/A snv 8.3E-02 1
rs130516 22 33951570 intergenic variant A/G snv 0.73 1
rs13054906
DMC1
22 38542931 intron variant G/A;T snv 1
rs13057446
LOC105373030
22 38421454 intron variant G/A snv 6.9E-02 1
rs132571
CACNA1I
22 39580128 intron variant A/C;G snv 1
rs133885
MYO18B
1.000 0.120 22 25763322 missense variant G/A;C snv 0.55 1
rs136293
OSBP2
22 30793249 intron variant G/A;C snv 1
rs137156
EFCAB6-AS1 ; EFCAB6
22 43550596 intron variant C/T snv 0.11 1
rs139481
CHADL ; L3MBTL2
22 41231382 intron variant C/T snv 0.33 1
rs141389097
MPPED1
22 43492473 intron variant A/G snv 0.70 1
rs149401731
DEPDC5
22 31812413 intron variant C/T snv 2.4E-02 1
rs165655
COMT ; ARVCF
1.000 0.040 22 19970240 3 prime UTR variant G/A snv 0.56 1
rs1771149
MED15
22 20529162 intron variant T/C;G snv 0.81 1