{{Rsnum
|rsid=121908819
|Gene=TMEM127
|Chromosome=2
|position=96265174
|Orientation=minus
|GMAF=0.001837
|Gene_s=TMEM127
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ClinVar
|rsid=121908819
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=96930912
|CHROM=2
|GMAF=0.0018
|dbSNPBuildID=133
|SSR=0
|SAO=3
|VP=0x050068020a01040016110120
|GENEINFO=TMEM127:55654; CIAO1:9391
|GENE_NAME=TMEM127; CIAO1
|GENE_ID=55654; 9391
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.96930912C>T
|CLNORIGIN=2
|CLNSIG=4
|CLNCUI=171300
|CLNDBN=Pheochromocytoma
|Tags=RV;PM;PMC;NSM;REF;R5;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9982; 0.001837
|CLNDSDB=OMIM
|CLNDSDBID=171300
|COMMON=1
|Disease=Pheochromocytoma
}}{{PMID Auto
|PMID=21156949
|Title=Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas.
}}
{{omim
|id=171300
|rsnum=121908819
}}