{{Rsnum
|rsid=1668873
|Gene=TMCC2
|Chromosome=1
|position=205266862
|Orientation=minus
|GMAF=0.1942
|Gene_s=LOC100506871,TMCC2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 43.4 | 39.8 | 16.8
| HCB | 90.5 | 9.5 | 0.0
| JPT | 89.4 | 9.7 | 0.9
| YRI | 87.1 | 12.9 | 0.0
| ASW | 71.9 | 26.3 | 1.8
| CHB | 90.5 | 9.5 | 0.0
| CHD | 92.7 | 7.3 | 0.0
| GIH | 88.1 | 11.9 | 0.0
| LWK | 80.7 | 19.3 | 0.0
| MEX | 63.8 | 34.5 | 1.7
| MKK | 91.7 | 7.7 | 0.6
| TSI | 42.2 | 44.1 | 13.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19820697
|Trait=MPV
|Title=A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium
|RiskAllele=G
|Pval=1E-20
|OR=0.01
|ORtxt=[0.01-0.014] fl increase
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1668873
|overall_frequency_n=32
|overall_frequency_d=128
|overall_frequency=0.25
|n_genomes=22
|n_genomes_annotated=0
|n_haplomes=25
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

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