ClinVar Miner

List of variants reported as benign for autosomal dominant nonsyndromic hearing loss 10

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_004100.5(EYA4):c.*1264T>A rs9483585 0.99999
NM_004100.5(EYA4):c.*1434A>G rs9483586 0.79868
NM_004100.5(EYA4):c.829G>A (p.Gly277Ser) rs9493627 0.37885
NM_004100.5(EYA4):c.*23C>T rs3734279 0.35809
NM_004100.5(EYA4):c.*2108A>G rs17053541 0.24433
NM_004100.5(EYA4):c.*2184A>T rs17053542 0.20492
NM_004100.5(EYA4):c.*726C>A rs55805978 0.20466
NM_004100.5(EYA4):c.*1867C>T rs17053540 0.15248
NM_004100.5(EYA4):c.*3014T>C rs76510133 0.05509
NM_004100.5(EYA4):c.*1658C>T rs73546865 0.04226
NM_004100.5(EYA4):c.-76C>T rs78081370 0.04026
NM_004100.5(EYA4):c.*2302G>A rs41286208 0.02535
NM_004100.5(EYA4):c.*2685T>A rs41286210 0.01638
NM_004100.5(EYA4):c.905G>A (p.Gly302Asp) rs75133151 0.00860
NM_004100.5(EYA4):c.1845C>T (p.Asn615=) rs142721902 0.00854
NM_004100.5(EYA4):c.*1484C>T rs116238383 0.00723
NM_004100.5(EYA4):c.111T>C (p.Ser37=) rs35863035 0.00620
NM_004100.5(EYA4):c.103C>T (p.Leu35=) rs35562371 0.00597
NM_004100.5(EYA4):c.-445C>T rs112196731 0.00488
NM_004100.5(EYA4):c.*2918G>A rs75986250 0.00369
NM_004100.5(EYA4):c.-356T>C rs375432060 0.00104
NM_004100.5(EYA4):c.*2968T>A rs181492427
NM_004100.5(EYA4):c.-244C>G rs112173873
NM_004100.5(EYA4):c.-326C>G rs117602794

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