{{Rsnum
|rsid=80356673
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=NTRK1
|position=156860959
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NTRK1
}}{{omim
|id=191315
|rsnum=80356673
|variant=0005
}}{{ClinVar
|rsid=80356673
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=156860959
|CHROM=1
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168080605000002110100
|GENEINFO=NTRK1:4914
|GENE_NAME=NTRK1
|GENE_ID=4914
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.156860959C>T
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_001007792.1:c.123-3395C>T; NM_001012331.1:c.25C>T; NBK1769; 191315.0005
|CLNSIG=5
|CLNCUI=C0020074
|CLNDBN=Hereditary insensitivity to pain with anhidrosis
|Disease=Hereditary insensitivity to pain with anhidrosis
|CLNACC=RCV000030667.21; RCV000031917.1
|Tags=PM;PMC;SLO;NSN;REF;INT;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1769:C0020074:256800:ORPHA642:62985007
}}{{PMID Auto
|PMID=10330344
|Title=Congenital insensitivity to pain with anhidrosis: novel mutations in the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factor.
|OA=1
}}