{{Rsnum
|rsid=11906160
|Gene=MYH7B
|Chromosome=20
|position=34977952
|Orientation=plus
|GMAF=0.1423
|Gene_s=MYH7B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.9 | 21.2 | 77.9
| HCB | 0.0 | 13.1 | 86.9
| JPT | 0.9 | 9.8 | 89.3
| YRI | 5.4 | 41.5 | 53.1
| ASW | 7.0 | 45.6 | 47.4
| CHB | 0.0 | 13.1 | 86.9
| CHD | 1.9 | 25.9 | 72.2
| GIH | 2.0 | 25.7 | 72.3
| LWK | 4.5 | 51.8 | 43.6
| MEX | 5.3 | 12.3 | 82.5
| MKK | 7.1 | 43.9 | 49.0
| TSI | 1.0 | 20.6 | 78.4
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22216198
|Trait=None
|Title=A genome-wide association study of the Protein C anticoagulant pathway.
|RiskAllele=
|Pval=0.000001
|OR=None
|ORtxt=None
|OA=1
}}

{{GET Evidence
|gene=MYH7B
|aa_change=Ala25Thr
|aa_change_short=A25T
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs11906160
|overall_frequency_n=1649
|overall_frequency_d=10598
|overall_frequency=0.155595
|n_genomes=13
|n_genomes_annotated=0
|n_haplomes=12
|n_articles=0
|n_articles_annotated=0
|nblosum100=1
|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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}