List of variants in gene CYP4V2 reported as likely benign for corneal disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_207352.4(CYP4V2):c.327+11G>C	rs62350517	0.05079
NM_207352.4(CYP4V2):c.823G>A (p.Glu275Lys)	rs34745240	0.03921
NM_207352.4(CYP4V2):c.638G>A (p.Ser213Asn)	rs34331648	0.02714
NM_207352.4(CYP4V2):c.1091-4T>A	rs61748269	0.01211
NM_207352.4(CYP4V2):c.1536C>T (p.Gly512=)	rs72646298	0.01209

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