List of variants in gene MEN1 reported as likely benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001370259.2(MEN1):c.-22C>A	rs374749001	0.00073
NM_001370259.2(MEN1):c.1049+9C>T	rs200517349	0.00048
NM_001370259.2(MEN1):c.1080C>T (p.Ile360=)	rs147331514	0.00016
NM_001370259.2(MEN1):c.1508G>A (p.Gly503Asp)	rs375804228	0.00015
NM_001370259.2(MEN1):c.1638G>A (p.Pro546=)	rs368783097	0.00010
NM_001370259.2(MEN1):c.655-4del	rs748005956	0.00009
NM_001370259.2(MEN1):c.1032G>A (p.Thr344=)	rs760183888	0.00005
NM_001370259.2(MEN1):c.1695G>T (p.Leu565=)	rs767677287	0.00002
NM_001370259.2(MEN1):c.1404G>A (p.Glu468=)	rs755734265	0.00001
NM_001370259.2(MEN1):c.1608G>A (p.Gln536=)	rs1055457298	0.00001
NM_001370259.2(MEN1):c.1170G>C (p.Pro390=)	rs587780841
NM_001370259.2(MEN1):c.913-4C>T	rs770413697

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