List of variants in gene PRKG1 reported as benign by Ambry Genetics

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_006258.4(PRKG1):c.1008T>C (p.Phe336=)	rs56047641	0.05131
NM_006258.4(PRKG1):c.845A>G (p.Asn282Ser)	rs34997494	0.03846
NM_006258.4(PRKG1):c.888T>C (p.Leu296=)	rs113994747	0.02057
NM_006258.4(PRKG1):c.408G>A (p.Pro136=)	rs55806342	0.01754
NM_006258.4(PRKG1):c.1080T>C (p.Tyr360=)	rs141218982	0.00519
NM_006258.4(PRKG1):c.1525C>T (p.His509Tyr)	rs139646798	0.00109
NM_006258.4(PRKG1):c.675C>T (p.Thr225=)	rs142166726	0.00050
NM_006258.4(PRKG1):c.522C>T (p.Thr174=)	rs369697050

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