List of variants in gene GLB1 reported as 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000404.4(GLB1):c.325C>T (p.Arg109Trp)	rs35289681	0.01618
NM_000404.4(GLB1):c.1306C>T (p.Leu436Phe)	rs34421970	0.00952
NM_000404.4(GLB1):c.*319G>A	rs139730198	0.00851
NM_000404.4(GLB1):c.1577G>A (p.Gly526Asp)	rs147332381	0.00464
NM_000404.4(GLB1):c.76-4483G>A

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