ClinVar Miner

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

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_016169.4(SUFU):c.12G>A (p.Leu4=)	rs189234140	0.00425
NM_016169.4(SUFU):c.37A>C (p.Thr13Pro)	rs1456048322

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