Variant (rsID / SNP)

rs1047320

rs1047320 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LINS1. Location: chromosome 15, position 101,109,683. Clinical significance in the table: Likely benign.

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Reference-table entries

LINS1Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 15:101109683
Cytoband: 15q26.3
HGVS: NM_001040616.3(LINS1):c.2034A>G (p.Pro678=)
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.