List of variants in gene GIPC3 reported as likely benign for nonsyndromic genetic hearing loss

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_133261.3(GIPC3):c.57G>T (p.Ala19=)	rs754337950	0.00008
NM_133261.3(GIPC3):c.915C>T (p.Gly305=)	rs142749099	0.00003
NM_133261.3(GIPC3):c.69G>A (p.Ala23=)	rs150473323
NM_133261.3(GIPC3):c.706-3dup	rs200925508

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