{{Rsnum
|rsid=11085824
|Gene=GCDH
|Chromosome=19
|position=12890733
|Orientation=plus
|GMAF=0.2452
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=GCDH
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 41.6 | 46.0 | 12.4
| HCB | 72.3 | 25.5 | 2.2
| JPT | 70.8 | 27.4 | 1.8
| YRI | 74.7 | 24.7 | 0.7
| ASW | 68.4 | 26.3 | 5.3
| CHB | 72.3 | 25.5 | 2.2
| CHD | 74.3 | 22.9 | 2.8
| GIH | 52.5 | 41.6 | 5.9
| LWK | 70.6 | 27.5 | 1.8
| MEX | 27.6 | 39.7 | 32.8
| MKK | 73.1 | 26.3 | 0.6
| TSI | 49.0 | 38.2 | 12.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19862010
|Trait=Mean corpuscular hemoglobin
|Title=Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
|RiskAllele=G
|Pval=1E-11
|OR=0
|ORtxt=[0.003-0.005] pg decrease
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs11085824
|overall_frequency_n=23
|overall_frequency_d=128
|overall_frequency=0.179688
|n_genomes=16
|n_genomes_annotated=0
|n_haplomes=19
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

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