{{Rsnum
|rsid=9806762
|Gene=NTRK3
|Chromosome=15
|position=88118508
|Orientation=plus
|GMAF=0.332
|Gene_s=NTRK3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 44.2 | 45.1 | 10.6
| HCB | 59.9 | 35.8 | 4.4
| JPT | 58.4 | 37.2 | 4.4
| YRI | 27.2 | 53.1 | 19.7
| ASW | 24.6 | 49.1 | 26.3
| CHB | 59.9 | 35.8 | 4.4
| CHD | 46.8 | 39.4 | 13.8
| GIH | 43.6 | 44.6 | 11.9
| LWK | 32.7 | 46.4 | 20.9
| MEX | 51.7 | 39.7 | 8.6
| MKK | 41.9 | 43.2 | 14.8
| TSI | 45.1 | 42.2 | 12.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22388998
|Trait=None
|Title=Genome-wide association study of N370S homozygous Gaucher disease reveals the candidacy of CLN8 gene as a genetic modifier contributing to extreme phenotypic variation.
|RiskAllele=
|Pval=0.000007
|OR=None
|ORtxt=None
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}