ClinVar Miner

List of variants in gene KATNIP reported as likely benign by Genetic Services Laboratory, University of Chicago

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)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_015202.5(KATNIP):c.4745T>C (p.Met1582Thr)	rs145613851	0.00117
NM_015202.5(KATNIP):c.537G>C (p.Pro179=)	rs374427375

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