ClinVar Miner

List of variants in gene MEN1 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 42
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HGVS dbSNP gnomAD frequency
NM_001370259.2(MEN1):c.1621A>G (p.Thr541Ala) rs2959656 0.89377
NM_001370259.2(MEN1):c.912+283C>T rs504195 0.89058
NC_000011.10:g.64811334T>C rs149426934 0.44068
NC_000011.10:g.64811336T>C rs143462807 0.40104
NM_001370259.2(MEN1):c.1350+103G>C rs654440 0.32314
NM_001370259.2(MEN1):c.1254C>T (p.Asp418=) rs2071313 0.30843
NC_000011.10:g.64811338T>C rs199711128 0.28237
NM_001370259.2(MEN1):c.445+183G>A rs624975 0.12188
NM_001370259.2(MEN1):c.-23-16C>G rs509606 0.11597
NM_001370259.2(MEN1):c.1621= (p.Thr541=) rs2959656 0.10623
NM_130803.3(MEN1):c.-358T>C rs7949944 0.09264
NC_000011.10:g.64811551T>C rs10897528 0.09018
NM_130799.2(MEN1):c.-844C>T rs7934756 0.08485
NC_000011.10:g.64811340T>C rs1169663422 0.07751
NM_130803.3(MEN1):c.-43C>T rs11231874 0.07542
NC_000011.10:g.64811379T>G rs147112489 0.07528
NC_000011.10:g.64811375T>G rs145617061 0.06842
NC_000011.10:g.64811383T>G rs866352161 0.03087
NM_001370259.2(MEN1):c.435C>T (p.Ser145=) rs61736636 0.02784
NM_001370259.2(MEN1):c.1299= (p.His433=) rs540012 0.02405
NM_001370259.2(MEN1):c.*302C>T rs1804849 0.01607
NM_130803.3(MEN1):c.-33T>A rs650277 0.01572
NC_000011.10:g.64811367T>G rs2518905 0.01480
NM_001370259.2(MEN1):c.512G>A (p.Arg171Gln) rs607969 0.01309
NM_001370259.2(MEN1):c.654+82C>T rs114202287 0.00242
NM_001370259.2(MEN1):c.597C>T (p.His199=) rs150512958 0.00181
NM_001370259.2(MEN1):c.1296G>A (p.Leu432=) rs138770431 0.00119
NM_001370259.2(MEN1):c.30G>T (p.Leu10=) rs371192390 0.00111
NM_001370259.2(MEN1):c.913-42G>C rs529037188 0.00013
NM_001370259.2(MEN1):c.1170G>A (p.Pro390=) rs587780841 0.00003
NM_001370259.2(MEN1):c.1050-71G>A rs919026003 0.00001
NC_000011.10:g.64811306CA[12] rs1207317757
NC_000011.10:g.64811306CA[15] rs1207317757
NC_000011.10:g.64811306CA[16] rs1207317757
NC_000011.10:g.64811306CA[17] rs1207317757
NC_000011.10:g.64811371T>G rs139163950
NC_000011.10:g.64811382_64811388del rs869164525
NC_000011.10:g.64811384_64811388del rs869164525
NM_001370259.2(MEN1):c.*126C>T rs138595686
NM_001370259.2(MEN1):c.1049+115A>G rs669976
NM_001370259.2(MEN1):c.1050-65T>A rs537795635
NM_001370259.2(MEN1):c.655-6C>T rs77461664

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