{{Rsnum
|rsid=121908826
|Chromosome=2
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=TMEM127
|position=96254117
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TMEM127
}}{{omim
|id=613403
|rsnum=121908826
|variant=0001
}}{{ClinVar
|rsid=121908826
|Reversed=1
|FwdREF=A
|FwdALT=C
|REF=T
|ALT=G
|RSPOS=96919855
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050068000000000002110100
|GENEINFO=TMEM127:55654
|GENE_NAME=TMEM127
|GENE_ID=55654
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.96919855T>G
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|CLNACC=RCV000000127.2
|CLNDBN=Pheochromocytoma, susceptibility to
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=613403.0001
|Disease=Pheochromocytoma
}}{{PMID|20154675|OA=1
}} Germline mutations in TMEM127 confer susceptibility to pheochromocytoma.