List of variants in gene SUFU reported as likely benign for Medulloblastoma; Familial meningioma; Joubert syndrome 32; Basal cell nevus syndrome 2

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_016169.4(SUFU):c.1291T>C (p.Leu431=)	rs141950577	0.00487
NM_016169.4(SUFU):c.210T>C (p.Tyr70=)	rs35166585	0.00430
NM_016169.4(SUFU):c.690C>T (p.Gly230=)	rs775675385	0.00001

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