List of variants in gene MEN1 reported as uncertain significance by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 18

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HGVS	dbSNP	gnomAD frequency
NM_001370259.2(MEN1):c.1567G>A (p.Ala523Thr)	rs760683615	0.00001
NM_001370259.2(MEN1):c.655-5C>G	rs752563214	0.00001
NM_001370259.2(MEN1):c.119_124del (p.Val40_Leu41del)	rs386134248
NM_001370259.2(MEN1):c.1295T>C (p.Leu432Pro)	rs2136100876
NM_001370259.2(MEN1):c.1350G>C (p.Gln450His)	rs1592636161
NM_001370259.2(MEN1):c.153C>A (p.Asn51Lys)
NM_001370259.2(MEN1):c.227C>T (p.Thr76Ile)
NM_001370259.2(MEN1):c.35C>G (p.Pro12Arg)
NM_001370259.2(MEN1):c.417C>A (p.His139Gln)	rs386134254
NM_001370259.2(MEN1):c.638_639delinsAA (p.Ala213Glu)	rs1114167518
NM_001370259.2(MEN1):c.644_652delinsGCCCCT (p.Val215_Arg218delinsGlyProTrp)	rs386134257
NM_001370259.2(MEN1):c.654+18C>T	rs180737290
NM_001370259.2(MEN1):c.654+3A>T	rs1064793168
NM_001370259.2(MEN1):c.686G>A (p.Arg229His)	rs878855197
NM_001370259.2(MEN1):c.689G>T (p.Cys230Phe)
NM_001370259.2(MEN1):c.776T>C (p.Leu259Pro)	rs2136139920
NM_001370259.2(MEN1):c.830C>A (p.Pro277His)	rs1060499973
NM_001370259.2(MEN1):c.979T>G (p.Tyr327Asp)	rs1259383083

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