Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
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
rs6311
HTR2A
0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs121909231
PTEN
0.667 0.600 10 87961095 stop gained C/A;T snv 32
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs121909219
PTEN
0.689 0.400 10 87957915 stop gained C/A;T snv 25
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
rs4906902
GABRB3
0.724 0.200 15 26774621 intron variant A/G snv 0.15 14
rs112795301
FOXP1
0.776 0.160 3 70972634 stop gained G/A snv 13
rs6994992
NRG1
0.790 0.120 8 31638065 upstream gene variant C/A;T snv 13
rs1085308043
PTEN
0.763 0.200 10 87925511 splice acceptor variant A/G;T snv 12
rs2710102
CNTNAP2
0.790 0.120 7 147877298 intron variant A/G;T snv 12
rs121917893
NLGN3
0.807 0.160 X 71167508 missense variant C/T snv 10
rs3746544
SNAP25 ; SNAP25-AS1
0.790 0.120 20 10306436 3 prime UTR variant G/T snv 0.68 10
rs6269
COMT ; MIR4761
0.827 0.240 22 19962429 5 prime UTR variant A/G snv 0.38 10
rs397514679
SYN1
0.790 0.200 X 47574321 stop gained G/A snv 9
rs686
DRD1
0.807 0.080 5 175441697 3 prime UTR variant G/A;C;T snv 9
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
rs2268498
CAV3 ; OXTR
0.827 0.080 3 8770725 intron variant T/C snv 0.41 7