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: rs1559372512
rs1559372512
1.000 0.120 2 178461120 inframe deletion ACA/- delins
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs201326023
rs201326023
0.882 0.120 2 26458218 missense variant C/T snv 4.3E-05 1.4E-05
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs397515435
rs397515435
1.000 0.120 2 26480968 missense variant C/T snv 8.0E-06 7.0E-06
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs397515601
rs397515601
1.000 0.120 2 26467364 splice donor variant C/A snv 8.0E-06 8.4E-05
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs530821443
rs530821443
1.000 0.120 2 26458219 missense variant G/A snv 5.5E-06
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: rs753580324
rs753580324
1.000 0.120 2 26461763 stop gained G/A;C snv 4.4E-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: rs777476179
rs777476179
0.851 0.280 2 73448259 frameshift variant A/- del 1.4E-05
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1057517966
rs1057517966
0.925 0.160 3 69959325 stop gained C/T snv
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1060499733
rs1060499733
0.851 0.120 3 47846757 missense variant A/G snv
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1226171550
rs1226171550
1.000 0.120 3 121993717 frameshift variant C/- delins 4.0E-06
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: rs1559751245
rs1559751245
0.882 0.280 3 69959280 missense variant C/G snv
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1559875009
rs1559875009
1.000 0.120 3 122001311 stop gained C/A snv
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs775062249
rs775062249
1.000 0.120 3 121993365 stop gained G/A snv 3.6E-05 7.0E-06
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1553904404
rs1553904404
1.000 0.200 4 87615910 frameshift variant -/C ins
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: rs774517056
rs774517056
1.000 0.200 4 1807128 missense variant C/G;T snv
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1561441451
rs1561441451
1.000 0.200 5 90642715 stop gained G/T snv
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0
dbSNP: rs1561543496
rs1561543496
1.000 0.200 5 90694641 stop gained 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: rs1561790371
rs1561790371
1.000 0.200 5 90815669 stop gained G/T snv
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.700 0