Variant (rsID / SNP)

rs144605615

rs144605615 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to L1CAM. Clinical significance in the table: Benign.

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Reference-table entries

L1CAMBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Cytoband: Xq28
HGVS: NM_001278116.2(L1CAM):c.28C>T (p.Pro10Ser)
Allele change: Missense_P10S

Associated conditions / phenotypes

History of neurodevelopmental disorder|Spastic paraplegia

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.