{{Rsnum
|rsid=805303
|Gene=BAT3
|Chromosome=6
|position=31648589
|Orientation=minus
|GMAF=0.4444
|Gene_s=BAG6
|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 | 47.8 | 42.5 | 9.7
| HCB | 32.4 | 51.5 | 16.2
| JPT | 35.4 | 43.4 | 21.2
| YRI | 9.5 | 38.8 | 51.7
| ASW | 15.8 | 42.1 | 42.1
| CHB | 32.4 | 51.5 | 16.2
| CHD | 36.7 | 46.8 | 16.5
| GIH | 55.4 | 36.6 | 7.9
| LWK | 18.2 | 39.1 | 42.7
| MEX | 32.8 | 53.4 | 13.8
| MKK | 14.7 | 46.8 | 38.5
| TSI | 42.2 | 48.0 | 9.8
| HapMapRevision=28
}}{{PharmGKB
|RSID=rs805303
|Name_s=intron 6 c.552+88G>C, c.551+89A>C
|Gene_s=APOM, BAT3
|Feature=
|Evidence=PubMed ID:19837266
|Annotation=Risk or phenotype-associated allele, tested allele: unspecified; minor allele designation varies by ethnicity in dbSNP Phenotype: In 114 cases and 414 controls (n = 528), univariate analysis of disease association showed OR = 0.63 for heterozygote, OR = 0.50 for homozygous, versus homozygous wild type, in ALL, with P(trend) OR = 0.68, p = 0.02 using an additive model. Study size: 528. Study population/ethnicity: Childhood acute lymphoblastic leukemia (<=14 years) and healthy newborn controls (1988 to 1999) from South Wales in the United Kingdom. Significance metric(s): p = 0.02. Type of association: CO.
|Drugs=
|Drug Classes=
|Diseases=Precursor Cell Lymphoblastic Leukemia-Lymphoma
|Curation Level=Curated
|PharmGKB Accession ID=PA165110227
}}

{{PMID Auto GWAS
|PMID=21909115
|Trait=None
|Title=Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
|RiskAllele=G
|Pval=1E-10
|OR=0.0540
|ORtxt=[NR] % increase
|OA=1
}}

{{PMID|18204098}} Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX.

{{GET Evidence
|impact=pharmacogenetic
|qualified_impact=Insufficiently evaluated pharmacogenetic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs805303
|overall_frequency_n=54
|overall_frequency_d=128
|overall_frequency=0.421875
|n_genomes=35
|n_genomes_annotated=0
|n_haplomes=45
|n_articles=1
|n_articles_annotated=0
|in_pharmgkb=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}