List of variants in gene HSPD1 reported as likely benign for 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_002156.5(HSPD1):c.1216-9C>T	rs189395138	0.00361
NM_002156.5(HSPD1):c.561T>C (p.Ser187=)	rs141357756	0.00155
NM_002156.5(HSPD1):c.700+8C>T	rs185384719	0.00143
NM_002156.5(HSPD1):c.18A>G (p.Thr6=)	rs79630442	0.00059
NM_002156.5(HSPD1):c.732T>G (p.Val244=)	rs142108846	0.00024
NM_002156.5(HSPD1):c.1488A>G (p.Gln496=)	rs142434256	0.00011
NM_002156.5(HSPD1):c.794A>G (p.Asn265Ser)	rs149003485	0.00011
NM_002156.5(HSPD1):c.1434C>G (p.Thr478=)	rs199527127

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