List of variants in gene OCRL reported as likely benign by Fulgent Genetics, Fulgent Genetics

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000276.4(OCRL):c.439+3A>G	rs61752971	0.00248
NM_000276.4(OCRL):c.912T>G (p.Gly304=)	rs190659938	0.00022
NM_000276.4(OCRL):c.105G>A (p.Arg35=)	rs142321728	0.00020
NM_000276.4(OCRL):c.152A>G (p.His51Arg)	rs764804719	0.00020
NM_000276.4(OCRL):c.2415C>T (p.Tyr805=)	rs377180274	0.00014
NM_000276.4(OCRL):c.1587C>G (p.Ala529=)	rs375634816	0.00013
NM_000276.4(OCRL):c.284G>A (p.Arg95His)	rs770375201	0.00006
NM_000276.4(OCRL):c.2563G>A (p.Val855Ile)	rs376280495	0.00005
NM_000276.4(OCRL):c.375G>T (p.Glu125Asp)	rs773022942	0.00004
NM_000276.4(OCRL):c.200-11dup	rs765652296

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