{{Rsnum
|rsid=697739
|Gene=ATXN1
|Chromosome=6
|position=16741802
|Orientation=minus
|GMAF=0.4536
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ATXN1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 9.8 | 53.6 | 36.6
| HCB | 60.7 | 34.1 | 5.2
| JPT | 60.2 | 33.6 | 6.2
| YRI | 42.2 | 46.3 | 11.6
| ASW | 49.1 | 38.6 | 12.3
| CHB | 60.7 | 34.1 | 5.2
| CHD | 61.5 | 34.9 | 3.7
| GIH | 17.0 | 45.0 | 38.0
| LWK | 49.5 | 38.5 | 11.9
| MEX | 22.4 | 51.7 | 25.9
| MKK | 25.2 | 54.8 | 20.0
| TSI | 9.8 | 45.1 | 45.1
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=19451621
|Trait=Amyotrophic lateral sclerosis
|Title=Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis
|RiskAllele=A
|Pval=0.000004
|OR=2.04
|ORtxt=[1.18-2.90] years younger
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs697739
|overall_frequency_n=61
|overall_frequency_d=128
|overall_frequency=0.476562
|n_genomes=43
|n_genomes_annotated=0
|n_haplomes=57
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

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