Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs397514698
GNAQ
0.667 0.400 9 77797577 missense variant C/T snv 52
rs28934906
MECP2
0.716 0.320 X 154031355 missense variant G/A snv 46
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs886039469
KCNMA1-AS1 ; KCNMA1
0.701 0.560 10 76891709 missense variant T/C snv 35
rs28934907
MECP2
0.732 0.320 X 154032268 missense variant G/A;C snv 30
rs57095329
MIR3142HG
0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs63750231
PSEN1
0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs776746
CYP3A5 ; ZSCAN25
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72 21
rs80356616
KCNJ11
0.732 0.360 11 17387917 missense variant C/T snv 19
rs28935468
MECP2
0.732 0.240 X 154030912 missense variant G/A snv 17
rs61749721
MECP2
0.732 0.200 X 154031065 stop gained G/A snv 17
rs80356537
ATP1A3
0.752 0.320 19 41970405 missense variant C/A;G;T snv 17
rs1611115
DBH
0.732 0.280 9 133635393 upstream gene variant T/C snv 0.80 16
rs2606345
CYP1A1
0.732 0.360 15 74724835 intron variant C/A snv 0.46 16
rs80356624
KCNJ11
0.752 0.240 11 17387490 missense variant C/A;T snv 16
rs1064797102
OTUD6B-AS1 ; OTUD6B
0.827 0.120 8 91071136 splice acceptor variant A/G snv 15
rs1562927768
KMT2E
0.790 0.080 7 105101476 frameshift variant AAAGA/- delins 15
rs7103411
BDNF ; BDNF-AS
0.752 0.160 11 27678578 intron variant C/T snv 0.82 15
rs2516839
USF1
0.732 0.320 1 161043331 5 prime UTR variant C/T snv 0.49 14