ClinVar Miner

List of variants in gene CTU2 reported as uncertain significance for See cases

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001012759.3(CTU2):c.1510C>G (p.Leu504Val)	rs770524689	0.00004
NM_001012759.3(CTU2):c.1526A>G (p.Asp509Gly)	rs773387253	0.00001

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