List of variants in gene LHFPL5 reported as likely pathogenic for Autosomal recessive nonsyndromic hearing loss 67

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_182548.4(LHFPL5):c.1A>G (p.Met1Val)	rs1060499810
NM_182548.4(LHFPL5):c.200A>G (p.Tyr67Cys)
NM_182548.4(LHFPL5):c.300del (p.Phe100fs)
NM_182548.4(LHFPL5):c.53A>G (p.Tyr18Cys)

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