Variants in gene MEN1 with conflicting interpretations "uncertain significance" and "pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001370259.2(MEN1):c.1154C>T (p.Ala385Val)	rs1298484645	0.00001
NM_001370259.2(MEN1):c.1354C>T (p.Arg452Trp)	rs863224810	0.00001
NM_001370259.2(MEN1):c.1050-3C>G	rs2136111597
NM_001370259.2(MEN1):c.652C>T (p.Arg218Trp)	rs794728620
NM_001370259.2(MEN1):c.758C>T (p.Ser253Leu)	rs386134259

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