Variant (rsID / SNP)

rs1480040681

rs1480040681 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NF2. Location: chromosome 22, position 30,057,244. Clinical significance in the table: Uncertain significance.

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Reference-table entries

NF2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 22:30057244
Cytoband: 22q12.2
HGVS: NM_000268.4(NF2):c.726C>G (p.His242Gln)
Allele change: Missense_H242Q

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.