List of variants in gene MEN1 reported as 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: 11

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HGVS	dbSNP	gnomAD frequency
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.-23-16C>G	rs509606	0.11597
NM_001370259.2(MEN1):c.1621= (p.Thr541=)	rs2959656	0.10623
NM_001370259.2(MEN1):c.435C>T (p.Ser145=)	rs61736636	0.02784
NM_001370259.2(MEN1):c.1299= (p.His433=)	rs540012	0.02405
NM_001370259.2(MEN1):c.512G>A (p.Arg171Gln)	rs607969	0.01309
NM_001370259.2(MEN1):c.597C>T (p.His199=)	rs150512958	0.00181
NM_001370259.2(MEN1):c.1296G>A (p.Leu432=)	rs138770431	0.00119
NM_001370259.2(MEN1):c.30G>T (p.Leu10=)	rs371192390	0.00111
NM_001370259.2(MEN1):c.1170G>A (p.Pro390=)	rs587780841	0.00003

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