List of variants in gene STK11 reported as benign by Ambry Genetics

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_000455.5(STK11):c.375-49G>A	rs34928889	0.45190
NM_000455.5(STK11):c.465-51T>C	rs2075606	0.29935
NM_000455.5(STK11):c.290+36G>T	rs3764640	0.25746
NM_000455.5(STK11):c.374+24G>T	rs2075604	0.18985
NM_000455.5(STK11):c.920+7G>C	rs2075607	0.16357
NM_000455.5(STK11):c.816C>T (p.Tyr272=)	rs9282859	0.02603
NM_000455.5(STK11):c.264C>A (p.Ile88=)	rs56354945	0.02303
NM_000455.5(STK11):c.369G>A (p.Gln123=)	rs140112347	0.00636
NM_000455.5(STK11):c.825G>A (p.Pro275=)	rs202011521	0.00011
NM_000455.5(STK11):c.125G>T (p.Arg42Leu)	rs148830698	0.00006
NM_000455.5(STK11):c.827G>T (p.Gly276Val)	rs749927908	0.00004
NM_000455.5(STK11):c.1129G>A (p.Ala377Thr)	rs768870802	0.00001
NM_000455.5(STK11):c.863-4T>C	rs778853572	0.00001
NM_000455.5(STK11):c.290+1197C>T
NM_000455.5(STK11):c.464+17G>A	rs587782429
NM_000455.5(STK11):c.735-6_735-2del	rs759090799

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