List of variants in gene MEN1 reported by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_001370259.2(MEN1):c.1299T>C (p.His433=)	rs540012	0.97595
NM_001370259.2(MEN1):c.1621A>G (p.Thr541Ala)	rs2959656	0.89377
NM_001370259.2(MEN1):c.1254C>T (p.Asp418=)	rs2071313	0.30843
NM_001370259.2(MEN1):c.-22C>A	rs374749001	0.00073
NM_001370259.2(MEN1):c.511C>T (p.Arg171Trp)	rs143329068	0.00009
NM_001370259.2(MEN1):c.655-4del	rs748005956	0.00009
NM_001370259.2(MEN1):c.563C>T (p.Pro188Leu)	rs199706698	0.00005
NM_001370259.2(MEN1):c.1522C>A (p.Gln508Lys)	rs386833403	0.00002
NM_001370259.2(MEN1):c.1252G>A (p.Asp418Asn)	rs104894264
NM_001370259.2(MEN1):c.249_252del (p.Ile85fs)	rs587776841
NM_001370259.2(MEN1):c.307del (p.Leu103fs)	rs794728639
NM_001370259.2(MEN1):c.655-6C>A	rs77461664

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