{{Rsnum
|rsid=137852994
|Gene=ASPM
|Chromosome=1
|position=197093168
|Orientation=minus
|GMAF=0.001837
|Gene_s=ASPM
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{omim
|id=605481
|variant=0005
|rsnum=137852994
}}{{ClinVar
|rsid=137852994
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=197093168
|CHROM=1
|GMAF=0.0018
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050360000605000016110100
|GENEINFO=ASPM:259266
|GENE_NAME=ASPM
|GENE_ID=259266
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.197093168G>A
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_018136.4:c.9178C>T; NBK9587; 605481.0005
|CLNSIG=5
|CLNCUI=C1837501; C1837501
|CLNDBN=Primary autosomal recessive microcephaly 5
|Disease=Primary autosomal recessive microcephaly 5
|CLNACC=RCV000005248.1
|Tags=RV;PM;S3D;SLO;NSN;REF;ASP;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9982; 0.001837
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK9587:C1837501:608716:ORPHA2512
|COMMON=1
}}