{{Rsnum
|rsid=74435397
|Chromosome=12
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=EMG1
|position=6974427
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=EMG1
}}{{omim
|id=611531
|rsnum=74435397
|variant=0001
}}{{ClinVar
|rsid=74435397
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=7083589
|CHROM=12
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=EMG1:10436
|GENE_NAME=EMG1
|GENE_ID=10436
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.7083589A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=611531.0001
|CLNSIG=5
|CLNCUI=C1859405
|CLNDBN=Bowen-Conradi syndrome
|Disease=Bowen-Conradi syndrome
|CLNACC=RCV000000938.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1859405:211180:1270
}}