ClinVar Miner

List of variants in gene STK11 reported as likely benign for Hereditary breast ovarian cancer syndrome

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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_000455.5(STK11):c.1211C>T (p.Ser404Phe)	rs200078204	0.00051
NM_000455.5(STK11):c.615G>A (p.Ala205=)	rs532889728	0.00003

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