{{Rsnum
|rsid=1829883
|Chromosome=5
|position=99445399
|Orientation=plus
|GMAF=0.3871
|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 | 40.7 | 44.2 | 15.0
| HCB | 40.1 | 44.5 | 15.3
| JPT | 36.3 | 54.0 | 9.7
| YRI | 49.0 | 43.5 | 7.5
| ASW | 47.4 | 36.8 | 15.8
| CHB | 40.1 | 44.5 | 15.3
| CHD | 35.8 | 53.2 | 11.0
| GIH | 30.7 | 53.5 | 15.8
| LWK | 48.2 | 45.5 | 6.4
| MEX | 19.0 | 60.3 | 20.7
| MKK | 49.4 | 43.6 | 7.1
| TSI | 33.3 | 48.0 | 18.6
| 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=0.0000060000000000000002
|OR=NR
|ORtxt=NR
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1829883
|overall_frequency_n=44
|overall_frequency_d=128
|overall_frequency=0.34375
|n_genomes=27
|n_genomes_annotated=0
|n_haplomes=34
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

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