ClinVar Miner

List of variants in gene TTC21B reported 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
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_024753.5(TTC21B):c.1387C>T (p.Pro463Ser)	rs16851307	0.01326
NM_024753.5(TTC21B):c.3004C>G (p.Leu1002Val)	rs146496725	0.00517

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