Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 43
rs1800972
DEFB1
0.708 0.440 8 6877901 5 prime UTR variant C/G;T snv 0.79 16
rs11362
DEFB1
0.742 0.360 8 6877877 5 prime UTR variant C/T snv 0.43 0.40 13
rs1799946
DEFB1
0.732 0.360 8 6877909 5 prime UTR variant C/T snv 0.36 0.41 13
rs28931594
GJB2
0.790 0.280 13 20189434 missense variant C/A;T snv 9
rs1057517491
GJB2
0.776 0.240 13 20189448 frameshift variant C/- delins 8
rs28929485
GJB2
0.807 0.320 13 20189532 missense variant G/A;C snv 7
rs72561723
GJB2
0.790 0.240 13 20189448 missense variant C/T snv 8.0E-06 7
rs1457403673
KRT14
0.882 0.120 17 41586785 missense variant G/A snv 7.0E-06 4