Variant (rsID / SNP)

rs137854562

rs137854562 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NF1. Location: chromosome 17, position 29,562,641. 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: 17:29562641
Cytoband: 17q11.2
HGVS: NM_001042492.3(NF1):c.3721C>T (p.Arg1241Ter)
Allele change: Nonsense_R1241X

Associated conditions / phenotypes

Neurofibromatosis, type 1|Inborn genetic diseases

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.