List of variants in gene combination CYP4V2, LOC129993526 reported as uncertain significance for corneal disorder

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_207352.4(CYP4V2):c.24C>T (p.Leu8=)	rs202148693	0.00077
NM_207352.4(CYP4V2):c.-178C>T	rs886059279	0.00009
NM_207352.4(CYP4V2):c.-22C>G	rs894067959	0.00002
NM_207352.4(CYP4V2):c.-133G>T	rs562885669
NM_207352.4(CYP4V2):c.-199C>T	rs886059278
NM_207352.4(CYP4V2):c.-56C>G	rs886059280

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