List of variants in gene ADGRV1 reported as likely pathogenic for Rare genetic deafness

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_032119.4(ADGRV1):c.12101T>G (p.Phe4034Cys)	rs876657647	0.00001
NM_032119.4(ADGRV1):c.14365C>T (p.Arg4789Trp)	rs1131691924	0.00001
NM_032119.4(ADGRV1):c.10229_10231dup (p.Val3410dup)	rs397517418

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