{{Rsnum
|rsid=4774518
|Gene=DUOXA2
|Chromosome=15
|position=45117274
|Orientation=plus
|GMAF=0.0225
|Gene_s=DUOXA1,DUOXA2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{omim
|id=612772
|rsnum=4774518
|variant=0001
}}

{{ population diversity
| geno1 = (C;C)
| geno2 = (C;T)
| geno3 = 
| CEU | 96.7 | 3.3 | 0
| CHB | 95.6 | 4.4 | 0
| JPT | 86.7 | 13.3 | 0
| YRI | 100.0 | 0.0 | 0
}}

{{ClinVar
|rsid=4774518
|Reversed=0
|FwdREF=C
|FwdALT=G,T
|REF=C
|ALT=G,T
|RSPOS=45409472
|CHROM=15
|GMAF=0.0224
|dbSNPBuildID=111
|SSR=0
|SAO=1
|VP=0x050060000000150517110100
|GENEINFO=DUOXA1:90527; DUOXA2:405753
|GENE_NAME=DUOXA1; DUOXA2
|GENE_ID=90527; 405753
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.45409472C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=612772.0001
|CLNSIG=5
|CLNCUI=C0342196
|CLNDBN=Thyroglobulin synthesis defect
|Disease=Thyroglobulin synthesis defect
|CLNACC=RCV000000473.1
|Tags=PM;VLD;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.9775; 0.0225
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0342196:274900:95716:63127008
|COMMON=1
}}

{{on chip | HumanOmni1Quad}}