Variants in gene CYP4V2 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_207352.4(CYP4V2):c.1328G>A (p.Arg443Gln)	rs72646291	0.00306
NM_207352.4(CYP4V2):c.99G>A (p.Leu33=)	rs145611966	0.00169
NM_207352.4(CYP4V2):c.1446G>A (p.Ser482=)	rs141950964	0.00089
NM_207352.4(CYP4V2):c.367A>G (p.Met123Val)	rs149684063	0.00021
NM_207352.4(CYP4V2):c.*210dup	rs199938898
NM_207352.4(CYP4V2):c.1338C>G (p.Pro446=)	rs35524919
NM_207352.4(CYP4V2):c.1479C>T (p.Asn493=)	rs374270799

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