{{Rsnum
|rsid=10489087
|Chromosome=4
|position=13792792
|Orientation=plus
|GMAF=0.1644
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=LINC01182
|Gene_s=LINC01182
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 20.4 | 79.6
| HCB | 0.0 | 25.0 | 75.0
| JPT | 5.4 | 33.9 | 60.7
| YRI | 3.4 | 25.9 | 70.7
| ASW | 3.5 | 22.8 | 73.7
| CHB | 0.0 | 25.0 | 75.0
| CHD | 1.8 | 28.4 | 69.7
| GIH | 3.0 | 17.8 | 79.2
| LWK | 1.8 | 29.1 | 69.1
| MEX | 1.7 | 41.4 | 56.9
| MKK | 1.3 | 29.5 | 69.2
| TSI | 5.0 | 23.8 | 71.3
| 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=0.0000050000000000000004
|OR=NR
|ORtxt=NR
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs10489087
|overall_frequency_n=21
|overall_frequency_d=128
|overall_frequency=0.164062
|n_genomes=13
|n_genomes_annotated=0
|n_haplomes=15
|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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}