List of variants in gene PRKAG3 reported as benign

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_017431.4(PRKAG3):c.9C>T (p.Pro3=)	rs60578863	0.02181
NM_017431.4(PRKAG3):c.1332C>T (p.Ile444=)	rs73082940	0.00860
NM_017431.4(PRKAG3):c.618C>T (p.Phe206=)	rs74519931	0.00410
NM_017431.4(PRKAG3):c.633+10C>T	rs370486325	0.00113
NM_017431.4(PRKAG3):c.457C>G (p.Leu153Val)	rs35050588

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