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

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_012073.5(CCT5):c.1059G>A (p.Leu353=)	rs114634318	0.00353
NM_012073.5(CCT5):c.331+14A>T	rs201171003	0.00199
NM_012073.5(CCT5):c.1425C>T (p.Thr475=)	rs370529963	0.00021
NM_012073.5(CCT5):c.1005C>T (p.Ile335=)	rs1282889055	0.00001

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