List of variants in gene STK11 reported as uncertain significance by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 7

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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.920+5G>A	rs587780013	0.00008
NM_000455.5(STK11):c.125G>T (p.Arg42Leu)	rs148830698	0.00006
NM_000455.5(STK11):c.1226G>A (p.Arg409Gln)	rs587782364	0.00003
NM_000455.5(STK11):c.1258G>A (p.Ala420Thr)	rs762482152
NM_000455.5(STK11):c.143A>G (p.Lys48Arg)	rs766776431
NM_000455.5(STK11):c.838_839delinsGT (p.Pro280Val)	rs786205863

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