Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2430561
IFNG ; IFNG-AS1
0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs4696480
TLR2
0.716 0.400 4 153685974 intron variant T/A snv 0.45 19
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 14
rs3730358
AKT1
0.724 0.360 14 104780070 intron variant G/A;C snv 0.16; 4.0E-03 14
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 13
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
rs12273363
BDNF
0.807 0.120 11 27723312 intron variant T/C snv 0.16 11
rs956572
BCL2
0.742 0.280 18 63153338 intron variant A/G snv 0.65 11
rs1480380
HLA-DMB
0.763 0.360 6 32945469 intron variant C/T snv 0.11 10
rs694539
NNMT
0.776 0.200 11 114262697 intron variant C/T snv 0.21 10
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 9
rs1386483
TPH2
0.790 0.080 12 72018714 intron variant T/C snv 0.53 9
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 9
rs3771829
TACR1
0.790 0.120 2 75137019 intron variant C/G snv 0.11 9
rs4523957
SMG6 ; SRR
0.790 0.120 17 2305605 intron variant G/T snv 0.54 9
rs779867
GRM7
0.776 0.120 3 7442784 intron variant T/C;G snv 9
rs1516725
ETV5 ; DGKG
0.925 0.120 3 186106215 intron variant T/C snv 0.86 8
rs17173608
RARRES2
0.807 0.240 7 150339575 intron variant T/G snv 0.11 8
rs17518584
CADM2
0.827 0.160 3 85555773 intron variant C/T snv 0.50 8