Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2254298
CAV3 ; OXTR
0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs9357271
BTBD9
0.776 0.160 6 38398097 intron variant T/C snv 0.38 8
rs4565946
TPH2
0.827 0.080 12 71942989 intron variant C/A;G;T snv 7
rs10042486 0.882 0.040 5 63965502 intron variant C/T snv 0.58 4
rs13316193
CAV3 ; OXTR
0.882 0.040 3 8761057 intron variant T/C snv 0.45 4
rs1519480
BDNF-AS
0.925 0.040 11 27654165 intron variant C/T snv 0.54 4
rs9653711
LOC107985505 ; OLIG2
0.851 0.120 21 33029641 intron variant G/A;C snv 4
rs16965628
SLC6A4
0.882 0.040 17 30228407 intron variant G/C snv 0.14 3
rs2071592
ATP6V1G2-DDX39B ; ATP6V1G2 ; NFKBIL1
0.882 0.200 6 31547563 intron variant T/A;C snv 3
rs2097603
TXNRD2 ; COMT
0.882 0.040 22 19940569 intron variant G/A;T snv 3
rs2268493
CAV3 ; OXTR
0.882 0.040 3 8759154 intron variant T/C snv 0.25 3
rs11174202
TAFA2
0.925 0.040 12 61858476 intron variant A/G snv 0.49 2
rs2075507
COMT ; TXNRD2
0.925 0.040 22 19940569 intron variant G/A;T snv 2
rs2268490
CAV3 ; OXTR
1.000 0.040 3 8755399 intron variant C/T snv 0.18 2
rs237887
OXTR ; CAV3
1.000 0.040 3 8755356 intron variant G/A;C snv 2
rs2834070 0.925 0.040 21 33015144 intron variant G/T snv 0.24 2
rs301434
SLC1A1 ; SPATA6L
0.925 0.040 9 4582082 intron variant C/G;T snv 2
rs301979
SPATA6L ; SLC1A1
0.925 0.040 9 4576851 intron variant G/A;C snv 2
rs4271390
NECTIN1
0.925 0.120 11 119655426 intron variant T/C snv 0.68 2
rs4686301
CAV3 ; OXTR
1.000 0.040 3 8756900 intron variant C/T snv 0.27 2
rs4825476
GRIA3
0.925 0.040 X 123307628 intron variant G/A;C snv 2
rs4988462
POU1F1
0.925 0.120 3 87264203 intron variant C/T snv 0.31 2
rs75063949
CARMIL1
0.925 0.040 6 25590813 intron variant C/G snv 0.14 2
rs1148374
CDH2
1.000 0.040 18 28070318 intron variant T/A snv 0.31 1
rs11854486
TRPM7
1.000 0.040 15 50660473 intron variant T/C snv 7.3E-02 1