"WangQJ Lab, Chinese People's Liberation Army General Hospital"[submit - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 227009	NM_033056.4(PCDH15):c.4812G>T (p.Arg1604Ser)	PCDH15 (R1604S +8 more)	Single nucleotide variant (missense variant +1 more)	not provided +5 more	GBenign/Likely benign
Select item 1185087	NC_000010.11:g.53995649_54022892del	PCDH15	Deletion	Autosomal recessive nonsyndromic hearing loss 23	GLikely pathogenic
Select item 1185088	NM_001384140.1(PCDH15):c.2756del (p.Met919fs)	PCDH15 (M848fs +6 more)	Deletion (frameshift variant)	Autosomal recessive nonsyndromic hearing loss 23	GPathogenic

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