{{Rsnum
|rsid=11466112
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=NGF
|position=115286135
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NGF
}}{{ 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 | 99.1 | 0.9 | 0.0
| YRI | 99.3 | 0.7 | 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 | 97.3 | 2.7 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 99.0 | 1.0 | 0.0
| HapMapRevision=28
}}{{omim
|id=162030
|rsnum=11466112
|variant=0001
}}

{{ClinVar
|rsid=11466112
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=115286135
|CHROM=1
|dbSNPBuildID=120
|SSR=0
|SAO=1
|VP=0x050368000b15040503110110
|GENEINFO=NGF:4803
|GENE_NAME=NGF
|GENE_ID=4803
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.115286135G>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_002506.2:c.661C>T; 162030.0001
|CLNSIG=5
|CLNCUI=C0020075
|CLNDBN=Congenital sensory neuropathy with selective loss of small myelinated fibers
|Disease=Congenital sensory neuropathy with selective loss of small myelinated fibers
|CLNACC=RCV000015089.24
|Tags=RV;PM;PMC;S3D;SLO;NSM;REF;SYN;OTH;ASP;VLD;HD;GNO;OTHERKG;PH3;LSD;OM;NOC
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0020075:608654:ORPHA64752:128206006
}}

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

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