Variants in gene MEN1 with conflicting interpretations "likely pathogenic" and "likely benign"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 2

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HGVS	dbSNP	gnomAD frequency
NM_001370259.2(MEN1):c.1618C>T (p.Pro540Ser)	rs745404679	0.00012
NM_001370259.2(MEN1):c.1169C>T (p.Pro390Leu)	rs761102084	0.00001

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