Variant (rsID / SNP)

rs8192466

rs8192466 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BDNF. Location: chromosome 11, position 27,680,107. Clinical significance in the table: Uncertain significance.

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Reference-table entries

BDNFUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 11:27680107
Cytoband: 11p14.1
HGVS: NM_001709.5(BDNF):c.5C>T (p.Thr2Ile)
Allele change: Silent

Associated conditions / phenotypes

Congenital central hypoventilation|Obesity

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.