{{Rsnum
|rsid=9494145
|Chromosome=6
|position=135111414
|Orientation=plus
|GMAF=0.1905
|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 | 1.8 | 29.2 | 69.0
| HCB | 8.8 | 35.3 | 55.9
| JPT | 9.8 | 38.4 | 51.8
| YRI | 0.0 | 9.0 | 91.0
| ASW | 0.0 | 15.8 | 84.2
| CHB | 8.8 | 35.3 | 55.9
| CHD | 8.3 | 40.7 | 50.9
| GIH | 3.0 | 25.0 | 72.0
| LWK | 0.0 | 9.1 | 90.9
| MEX | 6.9 | 31.0 | 62.1
| MKK | 1.3 | 4.5 | 94.2
| TSI | 4.9 | 37.3 | 57.8
| HapMapRevision=28
}}{{PharmGKB
|RSID=rs9494145
|Name_s=
|Gene_s=-
|Feature=
|Evidence=PubMed ID:19198610
|Annotation=The SNP at 6q23, close to MYB, that showed suggestive association with eosinophil counts was also associated with atopic asthma (P = 2.4 x 10(-4)).
|Drugs=
|Drug Classes=
|Diseases=Asthma
|Curation Level=Curated
|PharmGKB Accession ID=PA163522163
}}

{{PMID Auto GWAS
|PMID=20927387
|Trait=None
|Title=A genome-wide association study of red blood cell traits using the electronic medical record
|RiskAllele=C
|Pval=3E-15
|OR=0.98
|ORtxt=[0.74-1.22] unit increase
|OA=1
}}

{{PMID Auto GWAS
|PMID=22423221
|Trait=None
|Title=A meta-analysis and genome-wide association study of platelet count and mean platelet volume in african americans.
|RiskAllele=T
|Pval=3E-9
|OR=8.1900
|ORtxt=None
|OA=1
}}

{{PMID Auto
|PMID=19860791
|Title=Genetic evidence for a role of IL33 in nasal polyposis.
}}

{{GET Evidence
|impact=pharmacogenetic
|qualified_impact=Insufficiently evaluated pharmacogenetic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs9494145
|overall_frequency_n=23
|overall_frequency_d=128
|overall_frequency=0.179688
|n_genomes=18
|n_genomes_annotated=0
|n_haplomes=20
|n_articles=2
|n_articles_annotated=2
|in_pharmgkb=Y
|autoscore=1
|webscore=N
}}

[[Persistant Fetal Hemoglobin]]

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}