ClinVar Miner

List of variants in gene PKN1 reported as likely benign for not specified

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_002741.5(PKN1):c.1042A>G (p.Met348Val)	rs200118271	0.00008
NM_002741.5(PKN1):c.1238A>G (p.Asn413Ser)	rs762968134	0.00002

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