List of variants in gene GLB1 reported as likely benign by Illumina Laboratory Services, Illumina

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000404.4(GLB1):c.1233+8T>C	rs13093698	0.21250
NM_000404.4(GLB1):c.1594A>G (p.Ser532Gly)	rs73826339	0.05158
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.*376C>G	rs147437116	0.00659
NM_000404.4(GLB1):c.756C>T (p.Phe252=)	rs142326197	0.00547
NM_000404.4(GLB1):c.*184G>A	rs143430374	0.00483
NM_000404.4(GLB1):c.1715A>G (p.Gln572Arg)	rs183126947	0.00013
NM_000404.4(GLB1):c.792+10G>T	rs79518579

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