ClinVar Miner

List of variants in gene TYROBP reported as uncertain significance for Memory impairment; Cerebellar atrophy; Parkinsonian disorder; Bradykinesia; Cerebral cortical atrophy; Caudate atrophy; Action tremor; Frontotemporal cerebral atrophy; Dementia

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)
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Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_003332.4(TYROBP):c.94G>A (p.Asp32Asn)	rs758290972	0.00006

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