Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1057519338
rs1057519338
0.882 X 110264571 stop gained G/A snv
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1131692230
rs1131692230
0.807 0.160 X 19353124 missense variant A/G snv
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1454033665
rs1454033665
1.000 0.160 X 83508494 stop gained G/A snv
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1556445736
rs1556445736
0.925 0.200 X 108667167 synonymous variant A/G snv
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1569280235
rs1569280235
X 83508802 stop gained C/T snv
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1569280385
rs1569280385
1.000 0.160 X 83509299 stop gained G/A snv
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs28934908
rs28934908
0.732 0.280 X 154031409 missense variant G/A;T snv 5.5E-06
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs765498367
rs765498367
0.925 X 110317643 stop gained A/G;T snv 1.2E-04 2.8E-05
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1555896285
rs1555896285
1.000 0.120 22 37725698 frameshift variant AG/- delins
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1569034190
rs1569034190
1.000 0.120 22 37710443 stop gained C/G snv
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1569040134
rs1569040134
1.000 0.120 22 37723382 missense variant C/T snv
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1569042693
rs1569042693
1.000 0.120 22 37726080 stop gained C/A snv
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1569042782
rs1569042782
1.000 0.120 22 37726189 frameshift variant CTGATCCCCCAAG/- delins
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1569046250
rs1569046250
1.000 0.120 22 37734627 stop gained G/T snv
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1569167607
rs1569167607
1.000 0.040 22 37973727 stop gained G/C snv
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1237955948
rs1237955948
1.000 0.120 21 42382235 splice acceptor variant C/A;T snv 8.0E-06
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1244688796
rs1244688796
0.925 0.200 21 34449584 stop gained C/T snv 4.0E-06
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1429442821
rs1429442821
1.000 0.120 21 42380116 splice donor variant C/T snv
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs758346045
rs758346045
1.000 0.080 21 34449497 stop gained G/A;T snv 2.0E-05; 8.0E-06
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs779124360
rs779124360
0.925 0.200 21 34449585 stop gained C/T snv 4.0E-06
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs786204841
rs786204841
1.000 21 36461002 missense variant C/T snv
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs373145711
rs373145711
0.732 0.520 20 32433408 stop gained C/T snv 2.0E-05 2.8E-05
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1568278651
rs1568278651
1.000 0.120 19 3589849 stop gained G/T snv
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1568546120
rs1568546120
1.000 0.160 19 45368993 splice acceptor variant C/A snv
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1568546252
rs1568546252
1.000 0.160 19 45369132 stop gained C/A snv
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0