Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3761549
FOXP3
0.724 0.480 X 49260888 intron variant G/A snv 9.6E-02 18
rs2280883
FOXP3
0.827 0.280 X 49252667 intron variant T/C snv 0.30 9
rs863223904
ALAS2
0.827 0.200 X 55014829 missense variant C/T snv 6.1E-06 4
rs80291436
VCX
1.000 0.080 X 7843706 missense variant T/A;C;G snv 4.9E-05; 0.19 3
rs2267531
GPC3
0.925 0.120 X 133986233 upstream gene variant G/A;C snv 2
rs1415125
LOC101928832
1.000 0.080 X 146868046 intergenic variant A/G snv 1
rs2064836 1.000 0.080 X 92628018 downstream gene variant A/G;T snv 1
rs4503258
FOXO4 ; CXorf65
1.000 0.080 X 71103387 3 prime UTR variant C/T snv 3.6E-02 1
rs5945919
LINC00630
1.000 0.080 X 102963359 intergenic variant A/G snv 0.20 1
rs752745942
AR
1.000 0.080 X 67711555 missense variant C/G;T snv 5.5E-06; 5.5E-06 1
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 80
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 45
rs1800206
PPARA
0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 34
rs2267437
DESI1 ; XRCC6
0.724 0.320 22 41620695 intron variant C/A;G snv 19
rs132770
DESI1 ; XRCC6
0.752 0.320 22 41621260 5 prime UTR variant A/G snv 0.83 14
rs5751129
XRCC6 ; DESI1
0.752 0.320 22 41619761 intron variant C/T snv 0.69 14
rs20551
EP300
0.752 0.320 22 41152004 missense variant A/G snv 0.31 0.23 10
rs132774
XRCC6
0.776 0.280 22 41635949 intron variant C/G snv 0.69 9
rs738791
MMP11
0.851 0.120 22 23775338 intron variant C/T snv 0.37 6
rs56228771
SGSM3 ; MRTFA
0.827 0.200 22 40410091 3 prime UTR variant -/GTCT;GTCTGTCT delins 5
rs8177832
APOBEC3G
0.851 0.160 22 39081561 missense variant A/G snv 5.9E-02 0.14 5
rs1012068
DEPDC5
0.827 0.160 22 31869917 intron variant T/G snv 0.37 4
rs131451
MMP11 ; LOC107985577
0.882 0.120 22 23771357 intron variant C/T snv 0.82 4
rs2896019
PNPLA3
0.790 0.160 22 43937814 intron variant T/G snv 0.20 4
rs5998152
DEPDC5
0.827 0.160 22 31867176 intron variant T/C snv 0.37 4