List of variants in gene combination LOC130004614, SUFU reported as uncertain significance for Medulloblastoma; Familial meningioma; Joubert syndrome 32; Basal cell nevus syndrome 2

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_016169.4(SUFU):c.26C>T (p.Ala9Val)	rs775491374	0.00001
NM_016169.4(SUFU):c.32G>A (p.Gly11Asp)	rs1227379293
NM_016169.4(SUFU):c.9G>C (p.Glu3Asp)

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