List of variants in gene GLB1 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_000404.4(GLB1):c.1784G>C (p.Arg595Pro)	rs199694629
NM_000404.4(GLB1):c.941T>G (p.Phe314Cys)	rs1699001242
NM_000404.4(GLB1):c.958G>A (p.Ala320Thr)	rs1698735097

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