Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs2254298
CAV3 ; OXTR
0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs2232365
FOXP3
0.716 0.480 X 49259429 intron variant T/C snv 16
rs4646536
CYP27B1
0.724 0.440 12 57764205 intron variant A/G snv 0.38 0.32 14
rs4906902
GABRB3
0.724 0.200 15 26774621 intron variant A/G snv 0.15 14
rs2710102
CNTNAP2
0.790 0.120 7 147877298 intron variant A/G;T snv 12
rs779867
GRM7
0.776 0.120 3 7442784 intron variant T/C;G snv 9
rs3796863
CD38
0.790 0.160 4 15848363 intron variant G/T snv 0.41 8
rs1799836
MAOB
0.790 0.160 X 43768752 intron variant T/A;C snv 0.43 7
rs2268498
CAV3 ; OXTR
0.827 0.080 3 8770725 intron variant T/C snv 0.41 7
rs6782011
GRM7
0.807 0.120 3 7457960 intron variant C/T snv 0.52 7
rs870142
STX18-AS1
0.851 0.120 4 4646320 intron variant C/G;T snv 7
rs10877969
AVPR1A
0.882 0.120 12 63153459 intron variant T/C snv 0.26 6
rs16835979
STX18-AS1
0.851 0.120 4 4633549 intron variant C/A snv 0.20 6
rs16976358
LINC00907
0.827 0.080 18 42611606 intron variant T/C snv 1.0E-02 6
rs1843809
TPH2
0.851 0.080 12 71954918 intron variant G/T snv 0.77 6
rs2168351
ST8SIA2
0.851 0.120 15 92440492 intron variant A/G snv 0.33 6
rs2745557
PACERR ; PTGS2
0.807 0.200 1 186680089 intron variant A/G snv 0.83 6
rs3784730
ST8SIA2
0.851 0.120 15 92443898 intron variant A/G snv 0.44 6
rs4774388
RORA
0.807 0.200 15 61174799 intron variant C/T snv 0.81 6
rs6449182
CD38
0.807 0.160 4 15778830 intron variant C/G snv 0.22 6
rs6824295
STX18-AS1
0.851 0.120 4 4612553 intron variant C/T snv 0.20 6
rs7341475
RELN
0.851 0.240 7 103764368 intron variant G/A snv 0.17 6