List of variants in gene STK11 reported as likely benign by Illumina Laboratory Services, Illumina

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.369G>A (p.Gln123=)	rs140112347	0.00636
NM_000455.5(STK11):c.*613C>T	rs543187681	0.00300
NM_000455.5(STK11):c.597+14del	rs536282050	0.00067
NM_000455.5(STK11):c.*353C>A	rs866183878	0.00031
NM_000455.5(STK11):c.*8C>T	rs587782259	0.00027
NM_000455.5(STK11):c.1194G>A (p.Ala398=)	rs184271025	0.00023
NM_000455.5(STK11):c.666C>T (p.Pro222=)	rs542189325	0.00005
NM_000455.5(STK11):c.615G>A (p.Ala205=)	rs532889728	0.00003
NM_000455.5(STK11):c.483_484del	rs545375742
NM_000455.5(STK11):c.597+21dup	rs534445875

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