{{Rsnum
|rsid=118204055
|Chromosome=7
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RBM28
|position=128330896
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RBM28
}}{{omim
|id=612074
|rsnum=118204055
|variant=0001
}}{{ClinVar
|rsid=118204055
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=127970949
|CHROM=7
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=RBM28:55131
|GENE_NAME=RBM28
|GENE_ID=55131
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.127970949A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=612074.0001
|CLNSIG=5
|CLNCUI=C2677535
|CLNDBN=Alopecia, neurologic defects, and endocrinopathy syndrome
|Disease=Alopecia
|CLNACC=RCV000000768.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2677535:612079:157954
}}