{{Rsnum
|rsid=104894955
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ZNF41
|position=47449438
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ZNF41
}}{{omim
|id=314995
|rsnum=104894955
|variant=0001
}}{{ClinVar
|rsid=104894955
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=47308837
|CHROM=X
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000a01000002110100
|GENEINFO=ZNF41:7592
|GENE_NAME=ZNF41
|GENE_ID=7592
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.47308837G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=314995.0001
|CLNSIG=5
|CLNCUI=CN069343
|CLNDBN=X-Linked Mental Retardation 89
|Disease=X-Linked Mental Retardation 89
|CLNACC=RCV000010414.1
|Tags=RV;PM;NSM;REF;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN069343:300848:777
}}