ClinVar Miner

List of variants in gene MEN1 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 41
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HGVS dbSNP gnomAD frequency
NM_001370259.2(MEN1):c.*307T>G rs1804848 0.00855
NM_130803.3(MEN1):c.-311A>T rs77701676 0.00833
NC_000011.10:g.64803369G>T rs565550938 0.00709
NM_130802.2(MEN1):c.-489G>A rs141719223 0.00516
NM_001370259.2(MEN1):c.1050-163T>C rs115859693 0.00415
NM_000244.4(MEN1):c.-40G>C rs552417059 0.00317
NM_001370259.2(MEN1):c.597C>T (p.His199=) rs150512958 0.00181
NM_001370259.2(MEN1):c.-20G>A rs386134244 0.00158
NM_001370259.2(MEN1):c.30G>T (p.Leu10=) rs371192390 0.00111
NM_001370259.2(MEN1):c.-22C>A rs374749001 0.00073
NM_001370259.2(MEN1):c.1049+9C>T rs200517349 0.00048
NM_001370259.2(MEN1):c.18C>T (p.Ala6=) rs369348210 0.00039
NM_001370259.2(MEN1):c.-6G>A rs768088337 0.00023
NM_001370259.2(MEN1):c.762G>A (p.Leu254=) rs199909967 0.00018
NM_001370259.2(MEN1):c.1080C>T (p.Ile360=) rs147331514 0.00016
NM_001370259.2(MEN1):c.1508G>A (p.Gly503Asp) rs375804228 0.00015
NM_001370259.2(MEN1):c.1351-4C>T rs764408631 0.00014
NM_001370259.2(MEN1):c.1409C>T (p.Pro470Leu) rs750112288 0.00012
NM_001370259.2(MEN1):c.1638G>A (p.Pro546=) rs368783097 0.00010
NM_001370259.2(MEN1):c.492C>T (p.Ala164=) rs146759807 0.00010
NM_001370259.2(MEN1):c.1185+12G>A rs373609932 0.00008
NM_001370259.2(MEN1):c.1003C>A (p.Arg335=) rs371364206 0.00006
NM_001370259.2(MEN1):c.1800G>T (p.Leu600=) rs148825200 0.00004
NM_001370259.2(MEN1):c.753C>T (p.Thr251=) rs763326062 0.00004
NM_001370259.2(MEN1):c.1479G>A (p.Pro493=) rs546721780 0.00003
NM_001370259.2(MEN1):c.1155G>A (p.Ala385=) rs201091135 0.00002
NM_001370259.2(MEN1):c.1404G>A (p.Glu468=) rs755734265 0.00001
NM_001370259.2(MEN1):c.300C>G (p.Ala100=) rs773136972 0.00001
NC_000011.10:g.64811306CA[13] rs1207317757
NC_000011.10:g.64811306CA[18] rs1207317757
NC_000011.10:g.64811351_64811361del rs1211855496
NC_000011.10:g.64811378_64811388del rs869164525
NC_000011.10:g.64811379_64811388del rs869164525
NC_000011.10:g.64811380_64811388del rs869164525
NM_000244.4(MEN1):c.-32G>C rs1021174779
NM_001370259.2(MEN1):c.1609G>A (p.Val537Met) rs1057521847
NM_001370259.2(MEN1):c.225C>A (p.Leu75=) rs1333791405
NM_001370259.2(MEN1):c.654+18C>T rs180737290
NM_001370259.2(MEN1):c.655-5dup rs772016629
NM_001370259.2(MEN1):c.655-6C>G rs77461664
NM_001370259.2(MEN1):c.825-10C>G rs999121619

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