{{Rsnum
|rsid=8192466
|Gene=BDNF
|Chromosome=11
|position=27658560
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|GMAF=0.001377
|Gene_s=BDNF,BDNF-AS
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 100.0 | 0.0 | 0.0
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 98.2 | 1.8 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{omim
|desc=CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL
|id=113505
|rsnum=8192466
|variant=0001
}}
{{ neighbor
| rsid = 6265
| distance = 191
}}

{{ClinVar
|rsid=8192466
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=27680107
|CHROM=11
|GMAF=0.0014
|dbSNPBuildID=117
|SSR=0
|SAO=1
|VP=0x050068000000040517110100
|GENEINFO=BDNF-AS:497258; BDNF:627
|GENE_NAME=BDNF-AS; BDNF
|GENE_ID=497258; 627
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.27680107G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=113505.0001
|CLNSIG=5
|CLNCUI=C1859049
|CLNDBN=Congenital central hypoventilation
|Disease=Congenital central hypoventilation
|CLNACC=RCV000019266.26
|Tags=RV;PM;PMC;VLD;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.9986; 0.001377
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1427:C1859049:209880:661:99803:399040002
|COMMON=0
}}

{{PMID Auto
|PMID=17212826
|Title=TAMGeS: a Three-array Method for Genotyping of SNPs by a dual-colour approach.
|OA=1
}}

{{PMID Auto
|PMID=17894414
|Title=BDNF Val66Met variant and age of onset in schizophrenia.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}