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: 3

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HGVS	dbSNP
NM_000244.3(MEN1):c.482G>A (p.Gly161Asp)	rs794728648
NM_000244.3(MEN1):c.518T>C (p.Leu173Pro)	rs386134256
NM_000244.3(MEN1):c.76G>A (p.Glu26Lys)	rs28931612

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