{{Rsnum
|rsid=7844723
|Chromosome=8
|position=121896264
|Orientation=plus
|GMAF=0.2925
|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 | 15.0 | 53.1 | 31.9
| HCB | 84.0 | 15.3 | 0.8
| JPT | 77.7 | 22.3 | 0.0
| YRI | 97.9 | 2.1 | 0.0
| ASW | 80.7 | 17.5 | 1.8
| CHB | 84.0 | 15.3 | 0.8
| CHD | 76.6 | 21.5 | 1.9
| GIH | 48.0 | 34.0 | 18.0
| LWK | 91.7 | 8.3 | 0.0
| MEX | 36.2 | 44.8 | 19.0
| MKK | 77.3 | 21.4 | 1.3
| TSI | 18.8 | 49.5 | 31.7
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=17903294
|Trait=Hemostatic factors and hematological phenotypes
|Title=Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study
|RiskAllele=
|Pval=0.0000019999999999999999
|OR=NR
|ORtxt=NR
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs7844723
|overall_frequency_n=38
|overall_frequency_d=128
|overall_frequency=0.296875
|n_genomes=25
|n_genomes_annotated=0
|n_haplomes=33
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}