List of variants in gene SUFU reported as likely pathogenic for Hereditary cancer-predisposing syndrome

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_016169.4(SUFU):c.597+1G>A	rs1590062006
NM_016169.4(SUFU):c.683+5G>A	rs2135870931
NM_016169.4(SUFU):c.739_756+12del	rs2545087054
NM_016169.4(SUFU):c.911-8C>A	rs771361493

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