ClinVar Miner

List of variants in gene combination CDK10, LINC02166 reported as uncertain significance for Al Kaissi syndrome

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_052988.5(CDK10):c.51T>G (p.Arg17=)	rs201507040	0.00060
NM_052988.5(CDK10):c.25G>C (p.Glu9Gln)	rs188849219

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