List of variants in gene SBF1 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_002972.4(SBF1):c.4833C>T (p.Asn1611=)	rs199573140	0.00247
NM_002972.4(SBF1):c.3856C>T (p.Leu1286=)	rs139035064	0.00100
NM_002972.4(SBF1):c.2396+7_2396+18del	rs570055395

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