Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 16
rs1130214
AKT1
0.742 0.280 14 104793397 5 prime UTR variant C/A snv 0.31 12
rs169068
SSTR5-AS1 ; SSTR5
0.742 0.280 16 1079872 missense variant C/T snv 0.54 0.50 12
rs3751143
P2RX7 ; LOC105370032
0.742 0.480 12 121184501 missense variant A/C;G snv 0.19; 4.0E-06 12
rs6971
TSPO
0.742 0.200 22 43162920 missense variant A/G snv 0.76 0.75 11
rs956572
BCL2
0.742 0.280 18 63153338 intron variant A/G snv 0.65 11
rs2230912
P2RX7 ; LOC105370032
0.752 0.280 12 121184393 missense variant A/G snv 0.13 0.12 16
rs821616
DISC1 ; TSNAX-DISC1
0.752 0.200 1 232008852 missense variant A/T snv 0.26 0.29 13
rs4988483
SSTR5-AS1 ; SSTR5
0.752 0.240 16 1079010 missense variant C/A snv 3.7E-02 3.7E-02 11
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs11030101
BDNF-AS ; BDNF
0.763 0.160 11 27659197 5 prime UTR variant A/T snv 0.36 10
rs1480380
HLA-DMB
0.763 0.360 6 32945469 intron variant C/T snv 0.11 10
rs1333045
CDKN2B-AS1
0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 14
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12
rs33388
NR3C1
0.776 0.360 5 143317730 intron variant A/T snv 0.53 12
rs694539
NNMT
0.776 0.200 11 114262697 intron variant C/T snv 0.21 10
rs886424
LINC00243
0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02 10
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 9
rs779867
GRM7
0.776 0.120 3 7442784 intron variant T/C;G snv 9
rs1469698992
NUP214
0.776 0.080 9 131190453 missense variant G/A snv 8
rs147837176
SLC6A3
0.776 0.080 5 1400949 missense variant T/C snv 3.1E-04 2.8E-04 8
rs1555454508
SPG11
0.790 0.240 15 44615487 stop gained GTA/ATC mnv 18
rs312262717
SPG11
0.790 0.240 15 44659104 frameshift variant A/-;AA delins 18
rs6994992
NRG1
0.790 0.120 8 31638065 upstream gene variant C/A;T snv 13