List of variants in gene MEN1 reported by Athena Diagnostics Inc

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 16

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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.1621= (p.Thr541=)	rs2959656	0.10623
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.1099G>A (p.Val367Ile)	rs758404089	0.00001
NM_001370259.2(MEN1):c.1252G>A (p.Asp418Asn)	rs104894264
NM_001370259.2(MEN1):c.1308G>T (p.Trp436Cys)	rs398124435
NM_001370259.2(MEN1):c.1546del (p.Arg516fs)	rs767319284
NM_001370259.2(MEN1):c.1546dup (p.Arg516fs)	rs767319284
NM_001370259.2(MEN1):c.202_206dup (p.Asp70fs)	rs730882136
NM_001370259.2(MEN1):c.249_252del (p.Ile85fs)	rs587776841
NM_001370259.2(MEN1):c.402del (p.Phe134fs)	rs397515385
NM_001370259.2(MEN1):c.586G>T (p.Val196Phe)
NM_001370259.2(MEN1):c.828C>A (p.Tyr276Ter)	rs1060503789
NM_001370259.2(MEN1):c.943del (p.Asp315fs)
NM_001370259.2(MEN1):c.959C>T (p.Pro320Leu)	rs1114167469

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