{{Rsnum
|rsid=10922162
|Gene=ASPM
|Chromosome=1
|position=197101646
|Orientation=plus
|GMAF=0.2897
|Gene_s=ASPM
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 74.1 | 23.2 | 2.7
| HCB | 16.3 | 40.7 | 43.0
| JPT | 11.7 | 45.0 | 43.2
| YRI | 97.9 | 2.1 | 0.0
| ASW | 87.7 | 12.3 | 0.0
| CHB | 16.3 | 40.7 | 43.0
| CHD | 5.5 | 43.1 | 51.4
| GIH | 52.0 | 34.0 | 14.0
| LWK | 98.2 | 1.8 | 0.0
| MEX | 42.1 | 36.8 | 21.1
| MKK | 91.0 | 9.0 | 0.0
| TSI | 72.5 | 26.5 | 1.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23381943
  |Trait=End-stage coagulation
  |Title=Ischemic stroke is associated with the ABO locus: the EuroCLOT study.
  |RiskAllele=C
  |Pval=2E-30
  |OR=.52
  |ORtxt=[0.43-0.61] unit increase
  |OA=1
}}

{{ClinVar
|ALT=T
|CAF=0.7103; 0.2897
|CHROM=1
|CLNACC=RCV000020793.1; RCV000123702.1
|CLNALLE=1
|CLNDBN=Primary autosomal recessive microcephaly 5; not provided
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK9587:C1837501:608716:ORPHA2512
|CLNHGVS=NC_000001.11:g.197101646C>T
|CLNSIG=2
|CLNSRC=ClinVar; GeneDx; GeneReviews
|CLNSRCID=NM_018136.4:c.7605G>A; 62469; NBK9587
|COMMON=1
|Disease=Primary autosomal recessive microcephaly 5; not provided
|FwdALT=T
|FwdREF=C
|GENEINFO=ASPM:259266
|GENE_ID=259266
|GENE_NAME=ASPM
|REF=C
|RSPOS=197101646
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;S3D;SLO;REF;SYN;INT;OTH;ASP;VLD;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD;MTP
|VC=SNV
|VP=0x05036808031515051f120100
|WGT=1
|dbSNPBuildID=120
|rsid=10922162
|CLNORIGIN=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}