{{Rsnum
|rsid=7159841
|Gene=MDGA2
|Chromosome=14
|position=47394632
|Orientation=plus
|GMAF=0.2971
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=MDGA2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 4.5 | 36.0 | 59.5
| HCB | 6.1 | 56.5 | 37.4
| JPT | 11.9 | 46.8 | 41.3
| YRI | 11.9 | 40.6 | 47.6
| ASW | 11.1 | 50.0 | 38.9
| CHB | 6.1 | 56.5 | 37.4
| CHD | 13.2 | 48.1 | 38.7
| GIH | 19.4 | 50.0 | 30.6
| LWK | 10.2 | 36.1 | 53.7
| MEX | 5.2 | 46.6 | 48.3
| MKK | 1.3 | 34.8 | 63.9
| TSI | 7.8 | 34.3 | 57.8
| 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=1.9999999999999999E-7
|OR=NR
|ORtxt=NR
|OA=1
}}

{{PMID Auto
|PMID=17903302
|Title=Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs7159841
|overall_frequency_n=92
|overall_frequency_d=126
|overall_frequency=0.730159
|n_genomes=48
|n_genomes_annotated=0
|n_haplomes=77
|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}}