List of variants in gene CYP4V2 reported as likely pathogenic by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_207352.4(CYP4V2):c.414-1G>A	rs767779208	0.00015
NM_207352.4(CYP4V2):c.1199G>A (p.Arg400His)	rs199476203	0.00003
NM_207352.4(CYP4V2):c.283G>C (p.Gly95Arg)

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