List of variants in gene CCDC88C reported as uncertain significance for Hydrocephalus, nonsyndromic, autosomal recessive 1; Spinocerebellar ataxia type 40

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001080414.4(CCDC88C):c.2393C>T (p.Ala798Val)	rs200650758	0.00081
NM_001080414.4(CCDC88C):c.6026C>T (p.Pro2009Leu)	rs201940261	0.00078
NM_001080414.4(CCDC88C):c.4579A>G (p.Thr1527Ala)	rs201414940	0.00057
NM_001080414.4(CCDC88C):c.590G>A (p.Arg197Gln)	rs200769097	0.00053
NM_001080414.4(CCDC88C):c.3404A>G (p.Gln1135Arg)	rs1407640264

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