Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913482
FGFR3
0.630 0.680 4 1801837 missense variant C/T snv 14
rs121913485
FGFR3
0.716 0.400 4 1804372 missense variant A/G snv 10
rs121913105
FGFR3
0.653 0.600 4 1806163 missense variant A/C;T snv 18
rs6773854
LOC105374265
1.000 0.120 3 187931631 downstream gene variant T/C snv 0.23 1
rs10190751
CFLAR-AS1 ; CFLAR
0.882 0.120 2 201141373 splice acceptor variant G/A snv 0.18 0.26 4
rs2274084
GJB2
0.882 0.240 13 20189503 missense variant C/T snv 5.4E-02 2.2E-02 6
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 118
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 107
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs10494879
IL19
0.925 0.120 1 206778859 intron variant C/A;G snv 0.36 3
rs6676671
IL19
0.882 0.160 1 206779403 intron variant T/A snv 0.32 4
rs2466571
CD46
0.925 0.120 1 207766701 intron variant G/T snv 0.46 3
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 135
rs1057519781
ALK
0.807 0.160 2 29209816 missense variant C/G snv 8
rs1346044
WRN
0.708 0.440 8 31167138 missense variant T/C snv 0.24 0.23 23
rs3099844
MICB-DT
0.732 0.400 6 31481199 non coding transcript exon variant C/A snv 0.11 5
rs2071286
NOTCH4
0.752 0.280 6 32212119 intron variant C/T snv 0.17 8
rs9268853
HLA-DRB9
0.790 0.440 6 32461866 intron variant T/C snv 0.29 1
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 11
rs9461776
HLA-DRB1
0.763 0.240 6 32607958 intergenic variant A/G snv 8.8E-02 8
rs2621416 0.882 0.280 6 32774091 intergenic variant T/C snv 0.26 1
rs2231231
AQP3
0.851 0.240 9 33442988 non coding transcript exon variant A/C snv 0.67 0.69 5
rs535311760
TP73
0.925 0.120 1 3730979 missense variant G/A snv 1.2E-05; 8.2E-06 3