List of variants in gene APPL1 reported as likely benign for monogenic diabetes

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_012096.3(APPL1):c.256T>C (p.Leu86=)	rs147166062	0.00501
NM_012096.3(APPL1):c.1262C>T (p.Pro421Leu)	rs35776173	0.00300
NM_012096.3(APPL1):c.374-9C>T

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