{{Rsnum
|rsid=7189020
|Gene=ITFG3
|Chromosome=16
|position=254804
|Orientation=plus
|GMAF=0.405
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene_s=ITFG3
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 32.3 | 50.0 | 17.7
| HCB | 14.3 | 45.2 | 40.5
| JPT | 9.5 | 45.2 | 45.2
| YRI | 0.0 | 3.5 | 96.5
| ASW | 0.0 | 0.0 | 0.0
| CHB | 14.3 | 45.2 | 40.5
| 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
}}
{{PMID Auto GWAS
|PMID=19862010
|Trait=Mean corpuscular volume
|Title=Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
|RiskAllele=T
|Pval=2E-12
|OR=0
|ORtxt=[0.002-0.004] fl decrease
|OA=1
}}{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs7189020
|overall_frequency_n=83
|overall_frequency_d=128
|overall_frequency=0.648438
|n_genomes=46
|n_genomes_annotated=0
|n_haplomes=78
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}