List of variants in gene VPS37A reported as benign for complex hereditary spastic paraplegia

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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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.970-1604A>G	rs10110023	0.36222
NM_152415.3(VPS37A):c.202T>C (p.Leu68=)	rs11555738	0.22377
NM_152415.3(VPS37A):c.1053C>T (p.Asp351=)	rs2285269	0.22285
NM_152415.3(VPS37A):c.316-17T>C	rs117165264	0.01240
NM_152415.3(VPS37A):c.616A>T (p.Ile206Phe)	rs17502618	0.00682
NM_152415.3(VPS37A):c.315+14A>C	rs59713854	0.00537
NM_152415.3(VPS37A):c.24C>T (p.Thr8=)	rs146098391	0.00409
NM_152415.3(VPS37A):c.637A>G (p.Ile213Val)	rs17687375	0.00252
NM_152415.3(VPS37A):c.125+8G>A	rs145945235	0.00156
NM_152415.3(VPS37A):c.1176A>G (p.Gln392=)	rs117336150	0.00065
NM_152415.3(VPS37A):c.418C>T (p.Leu140=)	rs143689645	0.00021
NM_152415.3(VPS37A):c.417-17_417-15del
NM_152415.3(VPS37A):c.834A>G (p.Glu278=)	rs541623528

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