List of variants in gene SHARPIN reported as benign 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_030974.4(SHARPIN):c.880C>T (p.Pro294Ser)	rs34674752	0.03102
NM_030974.4(SHARPIN):c.1094G>A (p.Arg365His)	rs112552278	0.00407
NM_030974.4(SHARPIN):c.517+9G>T	rs199932176

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