List of variants in gene combination LOC105369149, SBF2 reported as likely 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_030962.4(SBF2):c.5037C>T (p.Arg1679=)	rs200784979	0.00048
NM_030962.4(SBF2):c.4932T>C (p.Ser1644=)	rs757095964	0.00002
NM_030962.4(SBF2):c.5409C>T (p.Ser1803=)	rs1852007851

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