List of variants in gene HPS6 reported as likely pathogenic for not provided

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_024747.6(HPS6):c.1999C>T (p.Arg667Ter)	rs373272174	0.00002
NM_024747.6(HPS6):c.1054_1055del (p.Arg352fs)	rs2540987497
NM_024747.6(HPS6):c.1692dup (p.Phe565fs)	rs1384342700

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