List of variants in gene MEN1 reported as likely benign by Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001370259.2(MEN1):c.1296G>A (p.Leu432=)	rs138770431	0.00119
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.762G>A (p.Leu254=)	rs199909967	0.00018
NM_001370259.2(MEN1):c.1185+19A>G	rs1456615213	0.00001
NM_001370259.2(MEN1):c.1392G>A (p.Ala464=)	rs754445482	0.00001
NM_001370259.2(MEN1):c.*3T>A
NM_001370259.2(MEN1):c.-13A>C
NM_001370259.2(MEN1):c.-23-13G>A	rs757883651
NM_001370259.2(MEN1):c.-23-15C>G
NM_001370259.2(MEN1):c.-46T>A
NM_001370259.2(MEN1):c.1050-137C>A
NM_001370259.2(MEN1):c.825-35dup	rs768710094

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