{{Rsnum
|rsid=28937590
|Gene=BCS1L
|Chromosome=2
|position=218661219
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=G
|GMAF=0.0
|Gene_s=BCS1L,ZNF142
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{omim
|desc=GRACILE SYNDROME
|id=603647
|rsnum=28937590
|variant=0005
}}

{{ClinVar
|rsid=28937590
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=219525942
|CHROM=2
|GMAF=0
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000016110100
|GENEINFO=ZNF142:7701; BCS1L:617
|GENE_NAME=ZNF142; BCS1L
|GENE_ID=7701; 617
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.219525942A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603647.0005
|CLNSIG=5
|CLNCUI=C1864002
|CLNDBN=GRACILE syndrome
|Disease=GRACILE syndrome
|CLNACC=RCV000006542.1
|Tags=PM;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=1; 0
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1864002:603358:53693
|COMMON=0
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}