Variant (rsID / SNP)

rs11466111

rs11466111 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NGF. Location: chromosome 1, position 115,829,178. Clinical significance in the table: Benign/Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

NGFBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:115829178
Cytoband: 1p13.2
HGVS: NM_002506.3(NGF):c.239G>A (p.Arg80Gln)
Allele change: Missense_R80Q

Associated conditions / phenotypes

Congenital sensory neuropathy with selective loss of small myelinated fibers

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.