{{Rsnum
|rsid=11065987
|Chromosome=12
|position=111634620
|Orientation=plus
|GMAF=0.1965
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 44.2 | 44.2 | 11.5
| HCB | 99.3 | 0.7 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 84.2 | 14.0 | 1.8
| CHB | 99.3 | 0.7 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 81.2 | 17.8 | 1.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 67.2 | 29.3 | 3.4
| MKK | 0.0 | 0.0 | 0.0
| TSI | 24.5 | 53.9 | 21.6
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=19862010
|Trait=Hematocrit
|Title=Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
|RiskAllele=G
|Pval=1E-12
|OR=0.17
|ORtxt=[0.12-0.22] % decrease
|OA=1
}}

{{PMID Auto GWAS
|PMID=20686565
|Trait=None
|Title=Biological, clinical and population relevance of 95 loci for blood lipids.
|RiskAllele=G
|Pval=2E-9
|OR=0.9700
|ORtxt=None
|OA=1
}}

{{PMID Auto
|PMID=21193429
|Title=Determinants of platelet count in humans.
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs11065987
|overall_frequency_n=25
|overall_frequency_d=128
|overall_frequency=0.195312
|n_genomes=20
|n_genomes_annotated=0
|n_haplomes=22
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

Babies who are rs11065987(G;G) are about 1.3 times more likely to be born with tetralogy of Fallot (TOF) http://blog.23andme.com/23andme-research/snpwatch/snpwatch-common-genetic-factors-associated-with-blue-babies/

{{PMID Auto GWAS
  |PMID=23297363
  |Trait=Tetralogy of Fallot
  |Title=Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot.
  |RiskAllele=G
  |Pval=8E-11
  |OR=1.34
  |ORtxt=[1.208-1.496]
  |OA=1
}}

{{PMID Auto GWAS
  |PMID=24262325
  |Trait=Coronary artery disease or ischemic stroke
  |Title=Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
  |RiskAllele=
  |Pval=4E-14
  |OR=NR
  |ORtxt=NR
  }}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}