{{Rsnum
|rsid=63750567
|Chromosome=5
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=OSMR
|position=38925231
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=OSMR
}}{{omim
|id=601743
|rsnum=63750567
|variant=0001
}}

{{ClinVar
|rsid=63750567
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=38925333
|CHROM=5
|dbSNPBuildID=130
|SSR=0
|SAO=1
|VP=0x050068000000000002110100
|GENEINFO=OSMR:9180
|GENE_NAME=OSMR
|GENE_ID=9180
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.38925333T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601743.0001
|CLNSIG=5
|CLNCUI=C0268397
|CLNDBN=Cutaneous amyloidosis
|Disease=Cutaneous amyloidosis
|CLNACC=RCV000008251.1
|Tags=PM;PMC;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0268397:105250:353220:282834007
}}

{{PMID Auto
|PMID=18179886
|Title=Oncostatin M receptor-beta mutations underlie familial primary localized cutaneous amyloidosis.
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}