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

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_016169.4(SUFU):c.-33C>T	rs201649559	0.00551
NC_000010.11:g.102503873G>A	rs186314614	0.00493
NM_016169.4(SUFU):c.12G>A (p.Leu4=)	rs189234140	0.00425
NC_000010.11:g.102503825C>A	rs373586559	0.00351
NM_016169.4(SUFU):c.50C>T (p.Ala17Val)	rs12780580	0.00023
NM_016169.4(SUFU):c.6G>T (p.Ala2=)	rs746555296	0.00021
NM_016169.4(SUFU):c.96G>C (p.Pro32=)	rs1483435746	0.00003
NM_016169.4(SUFU):c.60G>C (p.Pro20=)	rs1589969926

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