Variant (rsID / SNP)

rs41278851

rs41278851 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NF2. Location: chromosome 22, position 30,094,366. Clinical significance in the table: Benign.

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Reference-table entries

NF2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 22:30094366
Cytoband: 22q12.2
HGVS: NM_000268.4(NF2):c.*3575G>A
Allele change: Silent

Associated conditions / phenotypes

Neurofibromatosis, type 2

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.