ClinVar Miner

List of variants in gene TSFM 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_005726.6(TSFM):c.754G>A (p.Val252Ile)	rs114694283	0.01391
NM_005726.6(TSFM):c.796C>A (p.Leu266Ile)	rs62000432	0.00702

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