List of variants in gene combination LOC130059818, SPG7 reported as likely benign for Hereditary spastic paraplegia 7

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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: 13

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HGVS	dbSNP	gnomAD frequency
NM_003119.4(SPG7):c.9G>T (p.Val3=)	rs553241838	0.01255
NM_003119.4(SPG7):c.4G>A (p.Ala2Thr)	rs535030441	0.00136
NM_003119.4(SPG7):c.144T>G (p.Pro48=)	rs1286342932	0.00003
NM_003119.4(SPG7):c.33C>T (p.Leu11=)	rs1319347094	0.00001
NM_003119.4(SPG7):c.99C>T (p.Phe33=)	rs1331243813	0.00001
NM_003119.4(SPG7):c.16C>T (p.Leu6=)
NM_003119.4(SPG7):c.183+12C>A
NM_003119.4(SPG7):c.183+20G>T
NM_003119.4(SPG7):c.183+22dup
NM_003119.4(SPG7):c.19C>T (p.Leu7=)
NM_003119.4(SPG7):c.30C>T (p.Ala10=)
NM_003119.4(SPG7):c.37C>G (p.Arg13Gly)	rs923197967
NM_003119.4(SPG7):c.78C>A (p.Gly26=)

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