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

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000455.5(STK11):c.598-8C>T	rs373610101	0.00123
NM_000455.5(STK11):c.1194G>A (p.Ala398=)	rs184271025	0.00023
NM_000455.5(STK11):c.678C>T (p.Asn226=)	rs748832988	0.00005
NM_000455.5(STK11):c.464+10C>T	rs587782445	0.00003
NM_000455.5(STK11):c.480G>T (p.Leu160=)	rs1176365465	0.00001
NM_000455.5(STK11):c.486C>T (p.Asp162=)	rs1269329328
NM_000455.5(STK11):c.558C>T (p.Thr186=)	rs749563734
NM_000455.5(STK11):c.734+14C>A	rs763346212
NM_000455.5(STK11):c.747C>T (p.Thr249=)	rs759546076

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