List of variants in gene GLB1 reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_000404.4(GLB1):c.1594A>G (p.Ser532Gly)	rs73826339	0.05158
NM_000404.4(GLB1):c.1588C>T (p.Arg530Cys)	rs371397760	0.00095
NM_000404.4(GLB1):c.1426C>T (p.Leu476=)	rs113534264	0.00083
NM_000404.4(GLB1):c.1833G>A (p.Ser611=)	rs201755284	0.00066
NM_000404.4(GLB1):c.1347+10G>A	rs199538100	0.00028
NM_000404.4(GLB1):c.1095C>T (p.Ile365=)	rs200762972	0.00015
NM_000404.4(GLB1):c.858C>T (p.Thr286=)	rs770638519	0.00002
NM_000404.4(GLB1):c.681C>T (p.Phe227=)	rs780608544	0.00001
NM_000404.4(GLB1):c.1310A>G (p.Asn437Ser)	rs202237232
NM_000404.4(GLB1):c.1584A>C (p.Gly528=)
NM_000404.4(GLB1):c.246-16GT[2]
NM_000404.4(GLB1):c.733+42T>A	rs886038291
NM_000404.4(GLB1):c.76-4376G>A
NM_000404.4(GLB1):c.76-4414C>T
NM_000404.4(GLB1):c.76-4429G>A
NM_000404.4(GLB1):c.915G>T (p.Leu305Phe)	rs772986593

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