ClinVar Miner

List of variants in gene KNL1 reported as pathogenic for not provided

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_144508.5(KNL1):c.6416-13T>G	rs370035611	0.00041
NM_144508.5(KNL1):c.1810C>T (p.Gln604Ter)	rs2141720777

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