List of variants in gene PTPRQ reported as benign for Hearing loss, autosomal dominant 73

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_001145026.2(PTPRQ):c.1187-38T>A	rs7311413	0.86872
NM_001145026.2(PTPRQ):c.2272+15_2272+16insG	rs56929349	0.85402
NM_001145026.2(PTPRQ):c.1934T>A (p.Val645Asp)	rs10778752	0.84044
NM_001145026.2(PTPRQ):c.3155-34A>T	rs11114502	0.54055
NM_001145026.2(PTPRQ):c.2505C>G (p.Leu835=)	rs12824064	0.52337
NM_001145026.2(PTPRQ):c.2371C>A (p.Gln791Lys)	rs11114486	0.49400
NM_001145026.2(PTPRQ):c.5943-6T>C	rs1528289	0.08370
NM_001145026.2(PTPRQ):c.6115+23_6115+24dup	rs10652830	0.06545
NM_001145026.2(PTPRQ):c.1187-27dup	rs56351124
NM_001145026.2(PTPRQ):c.1882+16TTG[7]	rs58537253
NM_001145026.2(PTPRQ):c.6453+21C>T	rs1163041

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