List of variants in gene TUB reported as uncertain significance for retinal disorder

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_177972.3(TUB):c.164G>A (p.Arg55Gln)	rs371844684	0.00005
NM_177972.3(TUB):c.115AAG[2] (p.Lys41del)	rs749961508

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