List of variants in gene STK11 reported as likely benign by Institute for Biomarker Research, Medical Diagnostic Laboratories, L.L.C.

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000455.5(STK11):c.464+9G>A	rs376313955	0.00208
NM_000455.5(STK11):c.*460G>A	rs558582150	0.00147
NM_000455.5(STK11):c.598-8C>T	rs373610101	0.00123
NM_000455.5(STK11):c.1211C>T (p.Ser404Phe)	rs200078204	0.00051
NM_000455.5(STK11):c.1284G>A (p.Ser428=)	rs369097329	0.00035
NM_000455.5(STK11):c.825G>A (p.Pro275=)	rs202011521	0.00011
NM_000455.5(STK11):c.787T>C (p.Leu263=)	rs372378119	0.00010
NM_000455.5(STK11):c.*176C>T	rs1599934027	0.00001
NM_000455.5(STK11):c.*309G>A
NM_000455.5(STK11):c.*70C>G	rs1029333558

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