List of variants in gene SBF2 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_030962.4(SBF2):c.4533A>G (p.Thr1511=)	rs79251068	0.01066
NM_030962.4(SBF2):c.*112G>A	rs144513995	0.00201
NM_030962.4(SBF2):c.4128G>A (p.Ala1376=)	rs191964053	0.00017
NM_030962.4(SBF2):c.*1091G>A	rs182391972	0.00013

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