{{Rsnum
|rsid=80356677
|Gene=NTRK1
|Chromosome=1
|position=156879336
|Orientation=plus
|GMAF=0.0004591
|Gene_s=NTRK1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ClinVar
|rsid=80356677
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=156879336
|CHROM=1
|GMAF=0.0005
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000a05000016110100
|GENEINFO=NTRK1:4914
|GENE_NAME=NTRK1
|GENE_ID=4914
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.156879336G>T
|CLNSRC=ClinVar; GeneReviews
|CLNORIGIN=0
|CLNSRCID=NM_001007792.1:c.1912G>T; NBK1769
|CLNSIG=5
|CLNCUI=C0020074
|CLNDBN=Hereditary insensitivity to pain with anhidrosis
|Disease=Hereditary insensitivity to pain with anhidrosis
|CLNACC=RCV000020470.1
|Tags=PM;PMC;SLO;NSM;REF;ASP;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1769:C0020074:256800:ORPHA642:62985007
|COMMON=0
}}{{PMID Auto
|PMID=11668614
|Title=Congenital insensitivity to pain with anhidrosis (CIPA): novel mutations of the TRKA (NTRK1) gene, a putative uniparental disomy, and a linkage of the mutant TRKA and PKLR genes in a family with CIPA and pyruvate kinase deficiency.
}}