{{Rsnum
|rsid=2974942
|Gene=PPP1R3A
|Chromosome=7
|position=113879741
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.02479
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=PPP1R3A
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 100.0 | 0.0 | 0.0
| HCB | 99.3 | 0.7 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 80.3 | 19.0 | 0.7
| ASW | 87.5 | 10.7 | 1.8
| CHB | 99.3 | 0.7 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 80.9 | 17.3 | 1.8
| MEX | 0.0 | 0.0 | 0.0
| MKK | 82.7 | 16.7 | 0.6
| TSI | 98.0 | 2.0 | 0.0
| HapMapRevision=28
}}{{Venter SNP
|rsid=2974942
|allele=T
|frequency=1
|uid=1103652678506
|type=homozygous_SNP
|hugo=PPP1R3A
|ensembl gene=ENSG00000154415
|ensembl transcript=ENST00000284601
|sift=
|disease=Defects in PPP1R3A are a cause of insulin resistance.
}}

{{ neighbor
| rsid = 2974944
| distance = 77
}}

{{GET Evidence
|gene=PPP1R3A
|aa_change=Val451Met
|aa_change_short=V451M
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2974942
|overall_frequency_n=10432
|overall_frequency_d=10756
|overall_frequency=0.969877
|n_genomes=56
|n_genomes_annotated=0
|n_haplomes=105
|n_articles=0
|n_articles_annotated=0
|nblosum100=0
|autoscore=0
|webscore=N
}}

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