Variant (rsID / SNP)

rs267606599

rs267606599 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NF1. Location: chromosome 17, position 29,557,401. Clinical significance in the table: Pathogenic.

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Reference-table entries

NF1Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 17:29557401
Cytoband: 17q11.2
HGVS: NM_001042492.3(NF1):c.3113+1G>A
Allele change: Silent

Associated conditions / phenotypes

Neurofibromatosis, type 1|Tibial pseudarthrosis|Neurofibromatosis, type 1|Hereditary cancer-predisposing syndrome

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.