List of variants in gene STK11 reported as benign for Breast and/or ovarian cancer

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000455.5(STK11):c.816C>T (p.Tyr272=)	rs9282859	0.02603
NM_000455.5(STK11):c.264C>A (p.Ile88=)	rs56354945	0.02303
NM_000455.5(STK11):c.369G>A (p.Gln123=)	rs140112347	0.00636

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