{{Rsnum
|rsid=7732671
|Gene=PPARGC1B
|Chromosome=5
|position=149832680
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=C
|GMAF=0.1028
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=PPARGC1B
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 1.5 | 23.1 | 75.4
| HCB | 0.0 | 17.8 | 82.2
| JPT | 2.3 | 13.6 | 84.1
| YRI | 1.6 | 24.2 | 74.2
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 17.8 | 82.2
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{omim
|desc=OBESITY, VARIATION IN
|id=608886
|rsnum=7732671
|variant=0001
}}

{{ClinVar
|rsid=7732671
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=149212243
|CHROM=5
|GMAF=0.1035
|dbSNPBuildID=116
|SSR=0
|SAO=1
|VP=0x050168000000170517110100
|GENEINFO=PPARGC1B:133522
|GENE_NAME=PPARGC1B
|GENE_ID=133522
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.149212243G>C
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;PMC;SLO;VLD;G5A;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.8972; 0.1028
|CLNACC=RCV000002119.1
|CLNDBN=Obesity, variation in
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=608886.0001
|COMMON=1
|Disease=Obesity
}}

{{PMID Auto
|PMID=19166596
|Title=Circadian polymorphisms associated with affective disorders.
|OA=1
}}

{{GET Evidence
|gene=PPARGC1B
|aa_change=Ala203Pro
|aa_change_short=A203P
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs7732671
|overall_frequency_n=1181
|overall_frequency_d=10758
|overall_frequency=0.109779
|n_genomes=13
|n_genomes_annotated=0
|n_haplomes=14
|n_articles=0
|n_articles_annotated=0
|nblosum100=2
|autoscore=0
|webscore=N
}}

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