{{Rsnum
|rsid=2405657
|Chromosome=11
|position=97811564
|Orientation=plus
|GMAF=0.4096
|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 | 8.9 | 42.9 | 48.2
| HCB | 40.7 | 44.4 | 14.8
| JPT | 32.7 | 49.6 | 17.7
| YRI | 4.1 | 34.7 | 61.2
| ASW | 8.9 | 39.3 | 51.8
| CHB | 40.7 | 44.4 | 14.8
| CHD | 27.1 | 58.9 | 14.0
| GIH | 21.8 | 47.5 | 30.7
| LWK | 9.1 | 48.2 | 42.7
| MEX | 24.1 | 46.6 | 29.3
| MKK | 7.1 | 39.4 | 53.5
| TSI | 17.6 | 46.1 | 36.3
| 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=0.000003
|OR=1.19
|ORtxt=[NR]
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2405657
|overall_frequency_n=83
|overall_frequency_d=126
|overall_frequency=0.65873
|n_genomes=46
|n_genomes_annotated=0
|n_haplomes=70
|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 | Illumina Human 1M}}