List of variants in gene RIPOR2 reported as benign for Autosomal recessive nonsyndromic hearing loss 104

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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_001286445.3(RIPOR2):c.2811T>C (p.Ser937=)	rs9358804	0.74640
NM_001286445.3(RIPOR2):c.*7G>A	rs9358799	0.44982
NM_001286445.3(RIPOR2):c.2540G>A (p.Arg847Gln)	rs9461073	0.24950
NM_001286445.3(RIPOR2):c.3043+9T>A	rs9379693	0.12477

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