List of variants in gene PC 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001040716.2(PC):c.1022+154C>A	rs45625436	0.04358
NM_001040716.2(PC):c.2224-9T>G	rs45560936	0.03311
NM_001040716.2(PC):c.2580C>T (p.Asp860=)	rs45584036	0.01323
NM_001040716.2(PC):c.2619C>T (p.Asn873=)	rs2229745	0.01182
NM_001040716.2(PC):c.*13C>T	rs58032722	0.00173
NM_001040716.2(PC):c.616G>T (p.Val206Leu)	rs147945506	0.00126
NM_001040716.2(PC):c.52C>A (p.Arg18=)	rs144583275	0.00086
NM_001040716.2(PC):c.1401C>T (p.Asn467=)	rs45623237	0.00028

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