{{Rsnum
|rsid=104894346
|Chromosome=12
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=DHH
|position=49094511
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=DHH
}}{{omim
|id=605423
|rsnum=104894346
|variant=0001
}}{{ClinVar
|rsid=104894346
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=49488294
|CHROM=12
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=DHH:50846
|GENE_NAME=DHH
|GENE_ID=50846
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.49488294A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605423.0001
|CLNSIG=5
|CLNCUI=C2751325
|CLNDBN=46,XY gonadal dysgenesis, partial, with minifascicular neuropathy
|Disease=46
|CLNACC=RCV000005313.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1547:C2751325:607080:168563
}}