{{Rsnum
|rsid=104895476
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=NOD2
|position=50711057
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NOD2
}}{{omim
|id=605956
|rsnum=104895476
|variant=0009
}}{{ClinVar
|rsid=104895476
|Reversed=0
|FwdREF=C
|FwdALT=G,T
|REF=C
|ALT=G,T
|RSPOS=50744968
|CHROM=16
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=NOD2:64127
|GENE_NAME=NOD2
|GENE_ID=64127
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.50744968C>G
|CLNSRC=OMIM Allelic Variant; UnitÃ© mÃ©dicale des maladies autoinflammatoires
|CLNORIGIN=1
|CLNSRCID=605956.0009; 348
|CLNSIG=5
|CLNCUI=C1836122
|CLNDBN=Sarcoidosis, early-onset
|Disease=Sarcoidosis
|CLNACC=RCV000004964.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1836122:609464
}}{{PMID Auto
|PMID=15459013
|Title=Early-onset sarcoidosis and CARD15 mutations with constitutive nuclear factor-kappaB activation: common genetic etiology with Blau syndrome.
}}