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Variant (rsID / SNP)

rs368649260

NF1

rs368649260 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NF1. Location: chromosome 17, position 29,588,886. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

NF1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
17:29588886
Cytoband
17q11.2
HGVS
NM_001042492.3(NF1):c.4724+11A>G
Allele change
Silent

Associated conditions / phenotypes

Neurofibromatosis, type 1|Café-au-lait macules with pulmonary stenosis|Neurofibromatosis, familial spinal|Neurofibromatosis-Noonan syndrome|Hereditary cancer-predisposing syndrome

Public references

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