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: rs1057518810
rs1057518810
7 107663430 missense variant T/C snv 1.4E-05
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1057518840
rs1057518840
2 26476319 splice acceptor variant T/C snv
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1057519338
rs1057519338
0.882 X 110264571 stop gained G/A snv
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1477766714
rs1477766714
1.000 12 80339241 stop gained C/G;T snv
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1561590396
rs1561590396
5 146339801 missense variant C/T snv
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1564573788
rs1564573788
10 26125584 missense variant T/G snv
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1567939718
rs1567939718
17 74919981 frameshift variant -/C delins
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1567940507
rs1567940507
17 74920522 missense variant G/A 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: rs267606855
rs267606855
1.000 4 42893495 stop gained C/T snv
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs371777049
rs371777049
1.000 1 216325540 missense variant C/T snv 3.6E-05 3.5E-05
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs375759781
rs375759781
13 20189108 stop gained G/A;C snv 1.2E-05
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs751906778
rs751906778
1.000 12 65463154 splice acceptor variant G/A snv 1.2E-05
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs754472294
rs754472294
1.000 1 6460077 frameshift variant C/- del 4.0E-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: rs765574676
rs765574676
5 90627593 missense variant C/T snv 2.8E-05 7.0E-06
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs767255075
rs767255075
7 107700161 missense variant T/C;G snv 1.2E-05; 8.0E-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: rs147682682
rs147682682
1.000 0.040 3 69956496 stop gained G/A;T snv 1.2E-05 1.4E-05
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1559749017
rs1559749017
0.925 0.040 3 69956531 splice donor variant G/A 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: rs533297350
rs533297350
1.000 0.040 2 227010441 missense variant C/T snv 7.2E-05 3.5E-05
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs569681869
rs569681869
0.925 0.040 2 227059468 missense variant C/G snv 7.2E-05 3.5E-05
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs777103184
rs777103184
0.827 0.040 2 29073071 stop gained C/T snv 8.0E-06
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1554958045
rs1554958045
1.000 0.080 11 2445213 stop gained G/T snv
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 1.000 1 2017 2017