ClinVar Miner

List of variants reported as benign for Hydrocephalus, nonsyndromic, autosomal recessive 1

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Total variants: 9
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HGVS dbSNP gnomAD frequency
NM_001080414.4(CCDC88C):c.1527+128A>G rs1285766 0.98802
NM_001080414.4(CCDC88C):c.5975T>C (p.Leu1992Pro) rs941920 0.90936
NM_001080414.4(CCDC88C):c.4630+78G>T rs2277509 0.65846
NM_001080414.4(CCDC88C):c.3966+12G>A rs3742656 0.56935
NM_001080414.4(CCDC88C):c.3009A>G (p.Leu1003=) rs1970912 0.56314
NM_001080414.4(CCDC88C):c.60+8C>A rs3742654 0.41434
NM_001080414.4(CCDC88C):c.114C>T (p.Tyr38=) rs45437097 0.16963
NM_001080414.4(CCDC88C):c.4975C>A (p.Arg1659=) rs150512553 0.02576
NM_001080414.4(CCDC88C):c.61-85T>C rs1285844

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