List of variants in gene OCRL reported as likely benign 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000276.4(OCRL):c.439+3A>G	rs61752971	0.00248
NM_000276.4(OCRL):c.1291G>A (p.Asp431Asn)	rs137884245	0.00169
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.2177G>T (p.Gly726Val)	rs755071897	0.00013
NM_000276.4(OCRL):c.50G>C (p.Gly17Ala)	rs768913997	0.00005
NM_000276.4(OCRL):c.441G>A (p.Gly147=)	rs199624352	0.00003
NM_000276.4(OCRL):c.2244C>T (p.Tyr748=)	rs781297236	0.00002
NM_000276.4(OCRL):c.1128G>T (p.Leu376=)
NM_000276.4(OCRL):c.1522G>A (p.Val508Ile)
NM_000276.4(OCRL):c.1935C>A (p.Ile645=)	rs2124418968
NM_000276.4(OCRL):c.2235A>G (p.Leu745=)
NM_000276.4(OCRL):c.471T>G (p.Ser157=)	rs747396791
NM_000276.4(OCRL):c.945A>G (p.Gln315=)

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