List of variants in gene BLOC1S3 reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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_212550.5(BLOC1S3):c.478G>T (p.Val160Leu)	rs201502372	0.00193
NM_212550.5(BLOC1S3):c.17G>A (p.Arg6His)	rs145609489	0.00072
NM_212550.5(BLOC1S3):c.589G>C (p.Asp197His)	rs529880074	0.00003

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