{{Rsnum
|rsid=1473247
|Gene=RNF145
|Chromosome=5
|position=159176563
|Orientation=plus
|GMAF=0.4376
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=RNF145
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 4.4 | 35.4 | 60.2
| HCB | 6.6 | 51.8 | 41.6
| JPT | 20.4 | 50.4 | 29.2
| YRI | 68.0 | 27.9 | 4.1
| ASW | 35.1 | 49.1 | 15.8
| CHB | 6.6 | 51.8 | 41.6
| CHD | 13.8 | 43.1 | 43.1
| GIH | 17.0 | 49.0 | 34.0
| LWK | 57.3 | 38.2 | 4.5
| MEX | 34.5 | 48.3 | 17.2
| MKK | 41.7 | 44.2 | 14.1
| TSI | 8.8 | 41.2 | 50.0
| 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=C
|Pval=3E-7
|OR=0.01
|ORtxt=[0.004-0.012] fl decrease
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1473247
|overall_frequency_n=60
|overall_frequency_d=126
|overall_frequency=0.47619
|n_genomes=35
|n_genomes_annotated=0
|n_haplomes=51
|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}}