{{Rsnum
|rsid=72552758
|Chromosome=6
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=C4A
|position=32040919
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CYP21A2,TNXB
}}{{omim
|id=201910
|rsnum=72552758
|variant=0025
}}{{ClinVar
|rsid=72552758
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=32008696
|CHROM=6
|dbSNPBuildID=130
|SSR=0
|SAO=1
|VP=0x050260040a01000002110100
|GENEINFO=TNXB:7148; CYP21A2:1589
|GENE_NAME=TNXB; CYP21A2
|GENE_ID=7148; 1589
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.32008696G>A
|CLNORIGIN=1
|CLNSIG=4
|CLNCUI=201910
|CLNDBN=21-hydroxylase deficiency
|Tags=PM;S3D;NSM;REF;R3;OTHERKG;LSD;OM
|CLNDSDB=OMIM
|CLNDSDBID=201910
|Disease=21-hydroxylase deficiency
}}