List of variants in gene MBP reported as likely benign

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001025101.2(MBP):c.243C>T (p.His81=)	rs150638800	0.00064
NM_001025101.2(MBP):c.888C>T (p.Arg296=)	rs761965498	0.00003
NM_001025101.2(MBP):c.507G>A (p.Thr169=)	rs577730388
NM_001025101.2(MBP):c.867G>A (p.Lys289=)	rs572017418
NM_001025101.2(MBP):c.877A>C (p.Arg293=)	rs1599445391

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