{{Rsnum
|rsid=137852737
|Chromosome=5
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FAM134B
|position=16565788
|Gene_s=FAM134B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=613114
|variant=0003
|rsnum=137852737
}}{{ClinVar
|rsid=137852737
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=16565897
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=FAM134B:54463
|GENE_NAME=FAM134B
|GENE_ID=54463
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.16565897G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK49247; 613114.0003
|CLNSIG=5
|CLNCUI=C2751092
|CLNDBN=Hereditary sensory and autonomic neuropathy type IIB; Hereditary sensory and autonomic neuropathy type IIA
|Disease=Hereditary sensory and autonomic neuropathy type IIB; Hereditary sensory and autonomic neuropathy type IIA
|CLNACC=RCV000000358.1; RCV000020420.1
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK49247:C2751092:613115:970; NBK49247:C2752089:201300:970
}}
{{omim
|id=201300
|rsnum=137852737
}}