List of variants in gene MEN1 reported as likely benign by Counsyl

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001370259.2(MEN1):c.-20G>A	rs386134244	0.00158
NM_001370259.2(MEN1):c.30G>T (p.Leu10=)	rs371192390	0.00111
NM_001370259.2(MEN1):c.1409C>T (p.Pro470Leu)	rs750112288	0.00012
NM_001370259.2(MEN1):c.339C>T (p.Ser113=)	rs559635859	0.00011
NM_001370259.2(MEN1):c.492C>T (p.Ala164=)	rs146759807	0.00010
NM_001370259.2(MEN1):c.655-4del	rs748005956	0.00009
NM_001370259.2(MEN1):c.1170G>A (p.Pro390=)	rs587780841	0.00003
NM_001370259.2(MEN1):c.784-16C>T	rs754257177	0.00002
NM_001370259.2(MEN1):c.655-5dup	rs772016629

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