Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs539699299
SLC26A4 ; SLC26A4-AS1
0.851 0.160 7 107661725 missense variant C/A;G snv 4
rs1057517303
SLC26A4
0.925 0.160 7 107710192 stop gained T/A;C snv 3
rs111033318
SLC26A4
0.925 0.160 7 107702050 missense variant T/A snv 3
rs121908361
SLC26A4
0.882 0.160 7 107689156 stop gained A/G;T snv 3
rs121908364
SLC26A4
0.925 0.160 7 107689166 missense variant C/T snv 3
rs1241745103
SLC26A4
0.925 0.160 7 107701139 frameshift variant G/- del 7.0E-06 3
rs1554360358
SLC26A4
0.925 0.160 7 107698076 missense variant A/C snv 3
rs786204474
SLC26A4
0.925 0.160 7 107689130 missense variant C/T snv 7.0E-06 3
rs786204581
SLC26A4 ; SLC26A4-AS1
0.925 0.160 7 107663366 stop gained C/T snv 3
rs786204601
SLC26A4
0.925 0.160 7 107696014 frameshift variant T/- delins 3
rs786204739
SLC26A4
0.925 0.160 7 107698083 missense variant T/G snv 3
rs111033257
SLC26A4
0.925 0.160 7 107700162 missense variant G/A snv 1.4E-05 2
rs121908365
SLC26A4
0.925 0.160 7 107672230 missense variant T/A;C snv 2
rs1554354787
SLC26A4
0.925 0.160 7 107674188 missense variant T/C snv 2
rs1554359670
SLC26A4
0.925 0.160 7 107694650 missense variant C/A snv 2
rs397516413
SLC26A4
0.925 0.160 7 107690171 frameshift variant T/- delins 7.0E-06 2
rs397516414
SLC26A4
0.925 0.160 7 107690178 missense variant G/A snv 2
rs431905486
SLC26A4
0.925 0.160 7 107683531 frameshift variant -/A delins 2
rs1045933779
SLC26A4
1.000 0.160 7 107710150 missense variant T/C snv 7.0E-06 1
rs1057516243
SLC26A4
1.000 0.160 7 107698092 missense variant G/T snv 1
rs1057516354
SLC26A4
1.000 0.160 7 107690212 frameshift variant A/- del 1
rs1057516535
SLC26A4
1.000 0.160 7 107696030 splice donor variant TCAGTTGTGAGT/- delins 1
rs1057516634
SLC26A4 ; SLC26A4-AS1
1.000 0.160 7 107661696 frameshift variant A/- del 2.1E-05 1
rs1057516636
SLC26A4
1.000 0.160 7 107701988 frameshift variant C/- delins 1
rs1057516658
SLC26A4 ; SLC26A4-AS1
1.000 0.160 7 107663380 stop gained G/A snv 1