{{Rsnum
|rsid=9971637
|Chromosome=12
|position=17220805
|Orientation=plus
|GMAF=0.1253
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 8.9 | 91.1
| HCB | 0.0 | 13.2 | 86.8
| JPT | 0.9 | 17.7 | 81.4
| YRI | 15.0 | 51.7 | 33.3
| ASW | 12.5 | 51.8 | 35.7
| CHB | 0.0 | 13.2 | 86.8
| CHD | 0.0 | 17.4 | 82.6
| GIH | 1.0 | 9.9 | 89.1
| LWK | 8.3 | 36.7 | 55.0
| MEX | 0.0 | 7.1 | 92.9
| MKK | 7.7 | 39.4 | 52.9
| TSI | 1.0 | 9.8 | 89.2
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19734901
|Trait=Amyotrophic lateral sclerosis
|Title=Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis
|RiskAllele=
|Pval=0.000002
|OR=1.48
|ORtxt=[NR]
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs9971637
|overall_frequency_n=25
|overall_frequency_d=126
|overall_frequency=0.198413
|n_genomes=18
|n_genomes_annotated=0
|n_haplomes=22
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=2
|webscore=N
|n_web_uneval=4
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}