{{Rsnum
|rsid=7306642
|Gene=STAB2
|Chromosome=12
|position=103745256
|Orientation=plus
|GMAF=0.0753
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=STAB2
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 0.9 | 11.0 | 88.1
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 3.5 | 29.2 | 67.4
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.9 | 99.1
| GIH | 0.0 | 5.1 | 94.9
| LWK | 4.7 | 25.5 | 69.8
| MEX | 1.7 | 12.1 | 86.2
| MKK | 0.0 | 0.0 | 0.0
| TSI | 2.0 | 10.8 | 87.3
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21810271
|Trait=None
|Title=Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels.
|RiskAllele=A
|Pval=0.000003
|OR=0.3000
|ORtxt=[0.18-0.42] IU/dL increase
|OA=1
}}

{{GET Evidence
|gene=STAB2
|aa_change=Pro2039Thr
|aa_change_short=P2039T
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs7306642
|overall_frequency_n=1127
|overall_frequency_d=10758
|overall_frequency=0.104759
|n_genomes=8
|n_genomes_annotated=0
|n_haplomes=8
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.011
|nblosum100=4
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}