ClinVar Miner

List of variants in gene TNIK reported as likely benign by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

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_015028.4(TNIK):c.417+11A>C	rs141160238	0.01091
NM_015028.4(TNIK):c.124-18A>G	rs76246285	0.00699

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