List of variants in gene combination LOC130004614, SUFU reported as likely benign for not specified

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_016169.4(SUFU):c.-33C>T	rs201649559	0.00551
NM_016169.4(SUFU):c.6G>T (p.Ala2=)	rs746555296	0.00021
NM_016169.4(SUFU):c.-48C>G
NM_016169.4(SUFU):c.6G>A (p.Ala2=)	rs746555296

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