Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1061624
TNFRSF1B
0.776 0.320 1 12207208 3 prime UTR variant A/G snv 0.48 8
rs10399805
CHI3L1
0.851 0.240 1 203186870 upstream gene variant G/A;T snv 7
rs2274976
MTHFR
0.807 0.320 1 11790870 missense variant C/T snv 5.6E-02 4.2E-02 7
rs368705607
MIXL1
0.882 0.120 1 226225766 missense variant T/C;G snv 2.8E-05; 4.0E-06 7
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 7
rs6675281
DISC2 ; DISC1 ; TSNAX-DISC1 ; LOC105373170
0.827 0.080 1 231818355 missense variant C/T snv 0.11 0.14 7
rs766288
TSNAX-DISC1 ; TSNAX
0.790 0.080 1 231557942 intron variant G/T snv 0.40 7
rs10399931
CHI3L1
0.807 0.320 1 203186952 upstream gene variant T/A;C snv 6
rs2252865
RERE
0.851 0.040 1 8362616 intron variant T/C snv 0.72 6
rs2745557
PACERR ; PTGS2
0.807 0.200 1 186680089 intron variant A/G snv 0.83 6
rs2812393
TSNAX-DISC1 ; DISC1
0.807 0.080 1 231777927 intron variant G/C snv 0.61 6
rs5177
LRP8
0.851 0.120 1 53246063 3 prime UTR variant G/A;C snv 6
rs7211
TXNIP
0.827 0.200 1 145993449 3 prime UTR variant G/A;C;T snv 6
rs4130548
GIPC2 ; DNAJB4
1.000 0.040 1 77998184 intron variant T/C snv 0.25 5
rs6336
NTRK1
0.827 0.120 1 156879126 missense variant C/T snv 4.2E-02 3.7E-02 5
rs6691840
GRIK3
0.827 0.120 1 36859876 missense variant A/C;G snv 0.27; 9.2E-05 5
rs6694545 0.851 0.040 1 29964421 intergenic variant A/G snv 0.58 5
rs10494251
BCL9
0.851 0.040 1 147552120 intron variant C/T snv 5.8E-02 4
rs10759
RGS4
0.851 0.160 1 163076561 3 prime UTR variant G/A;T snv 4
rs1858232
NOS1AP
0.882 0.080 1 162334048 intron variant A/G;T snv 4
rs3737983
LRP8
0.851 0.120 1 53250744 missense variant G/A;T snv 0.40; 2.4E-05; 1.2E-05 4
rs3738401
DISC1 ; TSNAX-DISC1
0.882 0.080 1 231694549 missense variant G/A snv 0.30 0.26 4
rs6586354 0.851 0.040 1 234897489 intron variant G/A snv 0.25 4
rs6676671
IL19
0.882 0.160 1 206779403 intron variant T/A snv 0.32 4
rs672607
BCL9
0.851 0.040 1 147581540 intron variant G/A snv 0.12 4