Variants in gene FREM2 with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_207361.6(FREM2):c.5642-9T>C	rs148794835	0.00141
NM_207361.6(FREM2):c.2740T>G (p.Cys914Gly)	rs146685625	0.00127
NM_207361.6(FREM2):c.2367G>A (p.Pro789=)	rs140101984	0.00095
NM_207361.6(FREM2):c.177T>C (p.Gly59=)	rs370018440	0.00079
NM_207361.6(FREM2):c.2823C>T (p.Pro941=)	rs150154438	0.00079
NM_207361.6(FREM2):c.1250T>C (p.Leu417Pro)	rs571694324	0.00003
NM_207361.6(FREM2):c.3035_3040dup (p.Gly1012_Ser1013dup)	rs570476408
NM_207361.6(FREM2):c.6674A>G (p.Asn2225Ser)	rs143576067
NM_207361.6(FREM2):c.7520-10_7520-9insCT	rs1399473815

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