ClinVar Miner

List of variants reported as benign for hereditary sensory and autonomic neuropathy with spastic paraplegia by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

Included ClinVar conditions (1):

Hereditary sensory and autonomic neuropathy with spastic paraplegia

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Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_012073.5(CCT5):c.332-18C>G	rs11741923	0.01963
NM_012073.5(CCT5):c.437A>T (p.Glu146Val)	rs11557652	0.01601
NM_012073.5(CCT5):c.1086C>G (p.Ile362Met)	rs141675330	0.00491

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