{{Rsnum
|rsid = 28942098
|Gene = CDC73
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=1
|position=193122203
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CDC73,LOC101929160
}}{{omim
|desc=HYPERPARATHYROIDISM-JAW TUMOR SYNDROME
|id=607393
|rsnum=28942098
|variant=0001
}}

{{ClinVar
|rsid=28942098
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=193122203
|CHROM=1
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050060040a15000502110100
|GENEINFO=CDC73:79577; LOC101929160:101929160
|GENE_NAME=CDC73; LOC101929160
|GENE_ID=79577; 101929160
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.193122203G>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_024529.4:c.3G>A; 607393.0001
|CLNSIG=5
|CLNCUI=C1704981
|CLNDBN=Hyperparathyroidism 2
|Disease=Hyperparathyroidism 2
|CLNACC=RCV000003424.1
|Tags=PM;NSM;REF;R3;OTH;ASP;HD;GNO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK3789:C1704981:145001
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}