Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72474224
GJB2
0.708 0.440 13 20189473 missense variant C/A;T snv 7.7E-03 18
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs6903608
HLA-DRB9
0.742 0.400 6 32460508 intron variant C/G;T snv 11
rs371024165
GJB2
0.763 0.400 13 20189488 missense variant G/A;T snv 3.2E-05; 8.0E-06 9
rs4459895
LPP
0.827 0.160 3 188236626 intron variant A/C snv 0.88 5
rs111033243
SLC26A4
0.827 0.400 7 107689112 missense variant T/C snv 6.1E-04 8.1E-04 5
rs121908362
SLC26A4
0.882 0.280 7 107710132 missense variant A/G snv 1.2E-04 3.5E-05 5
rs9268528 0.851 0.280 6 32415331 regulatory region variant A/G snv 0.34 4
rs9268542 0.851 0.280 6 32416944 intergenic variant A/G snv 0.35 4
rs121908354
CDH23
0.882 0.240 10 71570884 missense variant C/T snv 4.0E-05 7.0E-06 4
rs2858870
HLA-DRB1
0.851 0.280 6 32604474 intergenic variant T/A;C snv 4
rs9269081
HLA-DRB9
0.851 0.280 6 32473323 intron variant A/C snv 0.69 4
rs3781093
GATA3
0.882 0.120 10 8059964 intron variant T/C snv 0.19 3
rs771494831
IFNL3
0.882 0.120 19 39244791 synonymous variant G/A snv 8.1E-06 3
rs483352866
TBC1D24
0.882 0.240 16 2496681 missense variant C/G;T snv 8.0E-06 3
rs768368875
TLR3
0.882 0.120 4 186076796 synonymous variant C/T snv 1.2E-05 3
rs6928977
AHI1
0.925 0.120 6 135305210 intron variant T/G snv 0.70 2
rs34972832
CLEC16A
0.925 0.120 16 11105081 intron variant G/A;T snv 0.14 2
rs1271250198
KCNQ4
0.925 0.240 1 40784233 missense variant T/C snv 2
rs13196329
TSBP1-AS1 ; TSBP1
0.925 0.120 6 32357594 intron variant A/C snv 2.6E-02 2
rs1311502646
NUP214
1.000 0.120 9 131178386 missense variant C/T snv 4.0E-06 1
rs112998813
UPF3A
1.000 0.120 13 114294254 intron variant T/C snv 6.8E-02 1