List of variants in gene L1CAM 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001278116.2(L1CAM):c.*383C>T	rs41311708	0.04318
NM_001278116.2(L1CAM):c.2872C>G (p.Leu958Val)	rs35902890	0.01086
NM_001278116.2(L1CAM):c.720G>A (p.Pro240=)	rs35151382	0.01040
NM_001278116.2(L1CAM):c.1977T>C (p.Pro659=)	rs143382184	0.00854
NM_001278116.2(L1CAM):c.36C>A (p.Leu12=)	rs140678848	0.00180
NM_001278116.2(L1CAM):c.2302G>A (p.Val768Ile)	rs36021462	0.00178
NM_001278116.2(L1CAM):c.2211G>A (p.Pro737=)	rs146782397	0.00035
NM_001278116.2(L1CAM):c.2657G>A (p.Arg886Gln)	rs142603269	0.00032
NM_001278116.2(L1CAM):c.1547-4T>A	rs200148275	0.00030
NM_001278116.2(L1CAM):c.113C>T (p.Thr38Met)	rs201151358	0.00027
NM_001278116.2(L1CAM):c.1293G>A (p.Ala431=)	rs137967792	0.00009
NM_001278116.2(L1CAM):c.1759G>C (p.Gly587Arg)	rs199888009	0.00008
NM_001278116.2(L1CAM):c.198-9C>T	rs782753470	0.00002
NM_001278116.2(L1CAM):c.1581A>C (p.Thr527=)	rs201131192

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