ClinVar Miner

List of variants in gene EYA4 reported as benign for autosomal dominant nonsyndromic hearing loss 10

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
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HGVS dbSNP gnomAD frequency
NM_004100.5(EYA4):c.829G>A (p.Gly277Ser) rs9493627 0.37885
NM_004100.5(EYA4):c.-76C>T rs78081370 0.04026
NM_004100.5(EYA4):c.905G>A (p.Gly302Asp) rs75133151 0.00860
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.-356T>C rs375432060 0.00104
NM_004100.5(EYA4):c.-244C>G rs112173873
NM_004100.5(EYA4):c.-326C>G rs117602794

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