List of variants in gene SUFU reported as uncertain significance 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_016169.4(SUFU):c.1105G>A (p.Val369Ile)	rs149449923	0.00006
NM_016169.4(SUFU):c.1023-4A>T
NM_016169.4(SUFU):c.134A>T (p.Tyr45Phe)	rs774611157
NM_016169.4(SUFU):c.1372C>T (p.Leu458Phe)	rs2492850467
NM_016169.4(SUFU):c.911-8C>T	rs771361493

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