List of variants in gene MEN1 reported as benign for Hereditary cancer-predisposing syndrome

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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: 22

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HGVS	dbSNP	gnomAD frequency
NM_001370259.2(MEN1):c.1254C>T (p.Asp418=)	rs2071313	0.30843
NM_001370259.2(MEN1):c.435C>T (p.Ser145=)	rs61736636	0.02784
NM_001370259.2(MEN1):c.512G>A (p.Arg171Gln)	rs607969	0.01309
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.1508G>A (p.Gly503Asp)	rs375804228	0.00015
NM_001370259.2(MEN1):c.1506G>C (p.Lys502Asn)	rs774296730	0.00014
NM_001370259.2(MEN1):c.913-42G>C	rs529037188	0.00013
NM_001370259.2(MEN1):c.1535C>T (p.Ser512Leu)	rs141679530	0.00011
NM_001370259.2(MEN1):c.1638G>A (p.Pro546=)	rs368783097	0.00010
NM_001370259.2(MEN1):c.655-4del	rs748005956	0.00009
NM_001370259.2(MEN1):c.1391C>T (p.Ala464Val)	rs778728934	0.00007
NM_001370259.2(MEN1):c.803A>G (p.Tyr268Cys)	rs773500082	0.00006
NM_001370259.2(MEN1):c.563C>T (p.Pro188Leu)	rs199706698	0.00005
NM_001370259.2(MEN1):c.1098A>T (p.Glu366Asp)	rs149383809	0.00004
NM_001370259.2(MEN1):c.1434C>T (p.Gly478=)	rs200280309	0.00004
NM_001370259.2(MEN1):c.1518C>T (p.Thr506=)	rs749265222	0.00004
NM_001370259.2(MEN1):c.1170G>A (p.Pro390=)	rs587780841	0.00003
NM_001370259.2(MEN1):c.1012C>G (p.Leu338Val)	rs759337318	0.00002
NM_001370259.2(MEN1):c.843G>C (p.Gly281=)	rs562620826	0.00001
NM_001370259.2(MEN1):c.655-6C>T	rs77461664

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