Variant (rsID / SNP)

rs141855950

rs141855950 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LINS1. Location: chromosome 15, position 101,109,904. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

LINS1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 15:101109904
Cytoband: 15q26.3
HGVS: NM_001040616.3(LINS1):c.1813A>G (p.Met605Val)
Allele change: Silent

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.