Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs688325
BCL9
0.851 0.040 1 147605490 intron variant G/A snv 0.19 4
rs781720548
CPNE1 ; RBM12
0.882 0.040 20 35652946 stop gained C/A snv 4
rs878567
HTR1A
0.882 0.040 5 63960164 intron variant A/C;G snv 4
rs9394309
FKBP5
0.851 0.040 6 35654004 intron variant G/A snv 0.74 4
rs947267
DAOA-AS1 ; DAOA
0.882 0.040 13 105487313 intron variant T/G snv 0.51 4
rs10503929
NRG1
0.925 0.040 8 32756465 missense variant T/C snv 0.13 0.13 3
rs11789399
LOC105376249
0.882 0.040 9 118597008 intergenic variant G/A;C snv 3
rs11989919
NRG1
0.882 0.040 8 32645107 intron variant T/C snv 0.10 3
rs12278912
NRGN
0.882 0.040 11 124742263 intron variant G/A snv 0.33 3
rs12966547
LOC105372125
0.827 0.040 18 55084786 intergenic variant G/A snv 0.39 3
rs1421292 0.925 0.040 13 105545886 intergenic variant T/A snv 0.39 3
rs16965628
SLC6A4
0.882 0.040 17 30228407 intron variant G/C snv 0.14 3
rs17236239
CNTNAP2
0.882 0.040 7 147885213 intron variant A/G snv 0.26 3
rs17512836
TCF4
0.925 0.040 18 55527730 intron variant T/C snv 2.2E-02 3
rs1800557
APP
0.925 0.040 21 25891795 missense variant G/A snv 4.0E-05 4.2E-05 3
rs2007044
CACNA1C
0.882 0.040 12 2235794 intron variant A/G snv 0.50 3
rs2074898
NDUFS7
1.000 0.040 19 1391362 intron variant A/C;G snv 3
rs2075984
TPTEP2-CSNK1E ; CSNK1E
0.882 0.040 22 38294883 intron variant C/A;G;T snv 3
rs2076369
PICK1
0.925 0.040 22 38067645 non coding transcript exon variant T/A;G snv 3
rs2097603
TXNRD2 ; COMT
0.882 0.040 22 19940569 intron variant G/A;T snv 3
rs2189814
GRM3
0.925 0.040 7 86702440 intron variant T/A;C snv 3
rs2344484 0.925 0.040 5 135540941 upstream gene variant A/G snv 0.47 3
rs237902
CAV3 ; OXTR
0.925 0.040 3 8767498 synonymous variant G/A snv 0.29 0.31 3
rs2433322
PDLIM5
0.925 0.040 4 94458590 intron variant A/G snv 0.37 3
rs2514218 0.925 0.040 11 113522272 regulatory region variant C/T snv 0.26 3