List of variants in gene STK11 reported as benign for female reproductive system neoplasm

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000455.5(STK11):c.842C>T (p.Pro281Leu)	rs121913322	0.00006
NM_000455.5(STK11):c.795G>A (p.Glu265=)	rs730881963	0.00004
NM_000455.5(STK11):c.1168G>A (p.Val390Met)	rs374078532	0.00002
NM_000455.5(STK11):c.1217C>T (p.Ala406Val)	rs748202003	0.00001

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