List of variants in gene PRKAA2 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_006252.4(PRKAA2):c.95-7T>C	rs187294561	0.00795
NM_006252.4(PRKAA2):c.939T>C (p.Ser313=)	rs41285004	0.00381
NM_006252.4(PRKAA2):c.789-4C>T	rs112086177	0.00192
NM_006252.4(PRKAA2):c.1399T>C (p.Leu467=)	rs17848599	0.00111

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