ClinVar Miner

List of variants in gene combination EYA4, TARID reported as benign for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
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HGVS dbSNP
NM_004100.5(EYA4):c.*1264T>A rs9483585
NM_004100.5(EYA4):c.*1434A>G rs9483586
NM_004100.5(EYA4):c.*1484C>T
NM_004100.5(EYA4):c.*1658C>T rs73546865
NM_004100.5(EYA4):c.*1867C>T rs17053540
NM_004100.5(EYA4):c.*2108A>G rs17053541
NM_004100.5(EYA4):c.*2184A>T rs17053542
NM_004100.5(EYA4):c.*2302G>A rs41286208
NM_004100.5(EYA4):c.*23C>T rs3734279
NM_004100.5(EYA4):c.*2685T>A
NM_004100.5(EYA4):c.*2918G>A
NM_004100.5(EYA4):c.*2968T>A rs181492427
NM_004100.5(EYA4):c.*3014T>C rs76510133
NM_004100.5(EYA4):c.*726C>A rs55805978
NM_004100.5(EYA4):c.1845C>T (p.Asn615=) rs142721902

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