List of variants in gene combination LOC130004614, SUFU reported as pathogenic for Hereditary cancer-predisposing syndrome

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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.37_53dup (p.Gly19fs)	rs2135597189
NM_016169.4(SUFU):c.37del (p.Thr13fs)
NM_016169.4(SUFU):c.71del (p.Pro24fs)	rs587776579
NM_016169.4(SUFU):c.71dup (p.Ala25fs)	rs587776579

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