ClinVar Miner

List of variants in gene MEN1 reported as uncertain significance for Multiple endocrine neoplasia

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Total variants: 24
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HGVS dbSNP
NM_130799.2(MEN1):c.*104C>T rs886048477
NM_130799.2(MEN1):c.*272T>C rs563783609
NM_130799.2(MEN1):c.*373G>C rs886048476
NM_130799.2(MEN1):c.*392G>A rs886048475
NM_130799.2(MEN1):c.*438C>T rs886048474
NM_130799.2(MEN1):c.*470A>G rs778272737
NM_130799.2(MEN1):c.*527G>T rs886048473
NM_130799.2(MEN1):c.*529A>G rs886048472
NM_130799.2(MEN1):c.*533C>T rs879327862
NM_130799.2(MEN1):c.*557C>A rs886048471
NM_130799.2(MEN1):c.*560G>T rs886048470
NM_130799.2(MEN1):c.*570C>A rs886048469
NM_130799.2(MEN1):c.*794G>A rs117705251
NM_130799.2(MEN1):c.*89G>A rs886048478
NM_130799.2(MEN1):c.-106T>C rs886048481
NM_130799.2(MEN1):c.-23-14G>C rs886048479
NM_130799.2(MEN1):c.-94G>A rs886048480
NM_130799.2(MEN1):c.1186-10C>T rs762303621
NM_130799.2(MEN1):c.1296G>A (p.Leu432=) rs138770431
NM_130799.2(MEN1):c.1535C>T (p.Ser512Leu) rs141679530
NM_130799.2(MEN1):c.1764G>A (p.Lys588=) rs373669288
NM_130799.2(MEN1):c.327A>C (p.Glu109Asp) rs773976527
NM_130799.2(MEN1):c.61C>A (p.Arg21Ser) rs541476418
NM_130799.2(MEN1):c.774G>C (p.Gln258His) rs374659656

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