ClinVar Miner

List of variants reported as benign for hereditary spastic paraplegia 53 by Genome-Nilou Lab

Included ClinVar conditions (1):

Hereditary spastic paraplegia 53

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_152415.3(VPS37A):c.1114-26G>C	rs3793427	0.38313
NM_152415.3(VPS37A):c.841+23G>A	rs3213601	0.37262
NM_152415.3(VPS37A):c.1053C>T (p.Asp351=)	rs2285269	0.22285

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