{{Rsnum
|rsid=121918609
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=STIL
|position=47251285
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=STIL
}}{{omim
|id=181590
|rsnum=121918609
|variant=0001
}}{{ClinVar
|rsid=121918609
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=47251285
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000605000002110100
|GENEINFO=STIL:6491
|GENE_NAME=STIL
|GENE_ID=6491
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.47251285G>A
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_001048166.1:c.3718C>T; NBK9587; 181590.0001
|CLNSIG=5
|CLNCUI=C2675187; C2675187
|CLNDBN=Primary autosomal recessive microcephaly 7
|Disease=Primary autosomal recessive microcephaly 7
|CLNACC=RCV000013813.21
|Tags=RV;PM;SLO;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK9587:C2675187:612703:ORPHA2512
}}