Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs1088967 0.851 0.080 X 127010099 intergenic variant T/A;C snv 4
rs17276588
MIRLET7F2 ; MIR98 ; HUWE1
0.882 0.120 X 53557457 intron variant G/A snv 9.0E-02 4.2E-02 4
rs199469669
MED12
0.925 0.080 X 71119403 missense variant G/A;C;T snv 2
rs5934683
GPR143
0.790 0.080 X 9783434 intron variant T/C snv 0.50 1
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 45
rs1801198
TCN2
0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 26
rs2267437
DESI1 ; XRCC6
0.724 0.320 22 41620695 intron variant C/A;G snv 19
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs3747093
YDJC
0.732 0.200 22 21630090 upstream gene variant G/A snv 0.32 14
rs2236142
HSCB ; CHEK2
0.827 0.120 22 28741956 5 prime UTR variant G/C snv 0.66 6
rs9620817
CHEK2
0.851 0.120 22 28712568 intron variant A/T snv 8.4E-02 4
rs150742660
NCAPH2 ; SCO2
0.925 0.080 22 50523735 missense variant A/G snv 8.0E-06 3
rs373001
MIR301B ; MIR130B
0.925 0.080 22 21653137 intron variant C/G;T snv 2
rs5762748
CHEK2
0.925 0.080 22 28694902 intron variant G/A snv 6.3E-02 2
rs5995355
NCF4-AS1
0.925 0.080 22 36855419 intron variant A/G;T snv 2
rs1165966405
PLA2G6
1.000 0.080 22 38169236 missense variant T/A;C snv 1.4E-05 1
rs361863
ISX
1.000 0.080 22 35067169 missense variant A/G snv 0.71 0.73 1
rs376497527
PLA2G6
1.000 0.080 22 38129537 missense variant G/C snv 7.0E-06 1
rs7286680
TCN2
1.000 0.080 22 30622574 intron variant T/G snv 0.36 1
rs777919630
CBS
0.623 0.680 21 43062358 missense variant G/A;T snv 8.0E-06; 4.0E-06 39
rs1237063529
CBS
0.752 0.360 21 43058894 missense variant T/G snv 5.6E-06 13
rs562625029
CBS
0.827 0.280 21 43058192 stop gained G/A snv 5
rs4998557
SOD1
0.851 0.080 21 31662579 intron variant G/A snv 0.22 4