List of variants in gene combination CP, HPS3 reported as likely benign for not specified

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_000096.4(CP):c.3182-4A>G	rs34272112	0.00805
NM_032383.5(HPS3):c.2472G>A (p.Ser824=)	rs201221505	0.00009
NM_032383.5(HPS3):c.2784A>G (p.Lys928=)

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