{{Rsnum
|rsid=104895461
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=NOD2
|position=50710912
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NOD2
}}{{omim
|id=605956
|rsnum=104895461
|variant=0004
}}{{ClinVar
|rsid=104895461
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=50744823
|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.50744823G>A
|CLNSRC=OMIM Allelic Variant; UnitÃ© mÃ©dicale des maladies autoinflammatoires
|CLNORIGIN=1
|CLNSRCID=605956.0004; 250
|CLNSIG=5
|CLNCUI=C1861303
|CLNDBN=Blau syndrome; Sarcoidosis, early-onset
|Disease=Blau syndrome; Sarcoidosis
|CLNACC=RCV000004958.1; RCV000084070.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet; MedGen:OMIM
|CLNDSDBID=C1861303:186580:90340; C1836122:609464
}}{{PMID|11528384}} CARD15 mutations in Blau syndrome.