List of variants in gene SUFU reported as pathogenic for not provided

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_016169.4(SUFU):c.436C>T (p.Arg146Ter)	rs1060501109	0.00001
NM_016169.4(SUFU):c.1022+1G>A	rs587776578
NM_016169.4(SUFU):c.1220_1221insT (p.Phe408fs)	rs2063697672
NM_016169.4(SUFU):c.225del (p.Asn76fs)	rs2544845660
NM_016169.4(SUFU):c.542_543dup (p.Asp182fs)	rs1590061914
NM_016169.4(SUFU):c.895C>T (p.Arg299Ter)	rs1590066162

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