Variants in gene MEN1 with conflicting interpretations "likely pathogenic" and "uncertain significance"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 17

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HGVS	dbSNP	gnomAD frequency
NM_001370259.2(MEN1):c.1618C>T (p.Pro540Ser)	rs745404679	0.00012
NM_001370259.2(MEN1):c.1169C>T (p.Pro390Leu)	rs761102084	0.00001
NM_001370259.2(MEN1):c.1354C>T (p.Arg452Trp)	rs863224810	0.00001
NM_001370259.2(MEN1):c.466G>A (p.Gly156Ser)	rs1085307471	0.00001
NM_001370259.2(MEN1):c.1063C>T (p.Arg355Trp)	rs863224807
NM_001370259.2(MEN1):c.1154C>T (p.Ala385Val)	rs1298484645
NM_001370259.2(MEN1):c.1185+1G>A	rs1941661315
NM_001370259.2(MEN1):c.1667AGA[1] (p.Lys557del)	rs794728661
NM_001370259.2(MEN1):c.35C>G (p.Pro12Arg)
NM_001370259.2(MEN1):c.430T>G (p.Phe144Val)	rs1114167543
NM_001370259.2(MEN1):c.526G>A (p.Ala176Thr)	rs376872829
NM_001370259.2(MEN1):c.639C>A (p.Ala213=)	rs746067825
NM_001370259.2(MEN1):c.652C>T (p.Arg218Trp)	rs794728620
NM_001370259.2(MEN1):c.654+3A>T	rs1064793168
NM_001370259.2(MEN1):c.758C>T (p.Ser253Leu)	rs386134259
NM_001370259.2(MEN1):c.818T>C (p.Leu273Pro)	rs1592647281
NM_001370259.2(MEN1):c.912G>T (p.Lys304Asn)	rs1592646211

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