ClinVar Miner

List of variants in gene CLPP reported as uncertain significance for Perrault syndrome 3

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_006012.4(CLPP):c.791T>C (p.Val264Ala)	rs112719208	0.00004
NM_006012.4(CLPP):c.520C>T (p.Arg174Cys)	rs1244525711	0.00001

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