List of variants in gene STK11 reported as likely pathogenic for digestive system disorder

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000455.5(STK11):c.291-2_374+91del	rs2145420502
NM_000455.5(STK11):c.582C>A (p.Asp194Glu)	rs786202134
NM_000455.5(STK11):c.582C>G (p.Asp194Glu)	rs786202134
NM_000455.5(STK11):c.719C>G (p.Ser240Trp)	rs730881976
NM_000455.5(STK11):c.853CTG[1] (p.Leu286del)	rs1057518830

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