ClinVar Miner

List of variants reported as benign for Hearing loss, autosomal recessive 107

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_012478.4(WBP2):c.305-5T>C	rs2290771	0.46485
NM_012478.4(WBP2):c.60-42C>T	rs936391	0.29127
NM_012478.4(WBP2):c.168+36T>C	rs936393	0.21034

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