Variant (rsID / SNP)

rs12460

rs12460 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LINS1. Location: chromosome 15, position 101,109,818. Clinical significance in the table: Benign.

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Reference-table entries

LINS1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 15:101109818
Cytoband: 15q26.3
HGVS: NM_001040616.3(LINS1):c.1899C>T (p.Asp633=)
Allele change: Silent

Associated conditions / phenotypes

History of neurodevelopmental disorder

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.