List of variants in gene combination LOC130004614, SUFU reported as benign for central nervous system neoplasm

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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.-178C>T	rs113962600	0.05045
NM_016169.4(SUFU):c.12G>A (p.Leu4=)	rs189234140	0.00425
NM_016169.4(SUFU):c.6G>T (p.Ala2=)	rs746555296	0.00021

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