List of variants in gene TRIOBP reported as uncertain significance for vestibular 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001039141.3(TRIOBP):c.5014G>T (p.Gly1672Ter)	rs200045032	0.00054
NM_001039141.3(TRIOBP):c.6560T>C (p.Leu2187Pro)
NM_001039141.3(TRIOBP):c.6911G>A (p.Arg2304Gln)

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