List of variants in gene MEN1 reported as not provided for parathyroid gland disorder

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001370259.2(MEN1):c.512G>A (p.Arg171Gln)	rs607969	0.01309
NM_001370259.2(MEN1):c.492C>T (p.Ala164=)	rs146759807	0.00010
NM_001370259.2(MEN1):c.1354C>T (p.Arg452Trp)	rs863224810	0.00001
NM_001370259.2(MEN1):c.1378C>T (p.Arg460Ter)	rs104894267	0.00001
NM_001370259.2(MEN1):c.1A>G (p.Met1Val)	rs386134250
NM_001370259.2(MEN1):c.652C>T (p.Arg218Trp)	rs794728620
NM_001370259.2(MEN1):c.936C>G (p.Tyr312Ter)	rs386134260

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