List of variants in gene STK11 reported as pathogenic for reproductive system disorder

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.388dup (p.Glu130fs)
NM_000455.5(STK11):c.488G>A (p.Gly163Asp)	rs137853078
NM_000455.5(STK11):c.812del (p.Ser271fs)	rs2145427067

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