{{Rsnum
|rsid=11099864
|Gene=FHDC1
|Chromosome=4
|position=152972202
|Orientation=plus
|GMAF=0.4541
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=FHDC1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 54.0 | 40.7 | 5.3
| HCB | 30.1 | 49.3 | 20.6
| JPT | 33.6 | 45.1 | 21.2
| YRI | 1.4 | 16.3 | 82.3
| ASW | 5.3 | 36.8 | 57.9
| CHB | 30.1 | 49.3 | 20.6
| CHD | 33.9 | 42.2 | 23.9
| GIH | 22.8 | 47.5 | 29.7
| LWK | 2.7 | 27.3 | 70.0
| MEX | 39.7 | 44.8 | 15.5
| MKK | 6.4 | 41.7 | 51.9
| TSI | 66.7 | 27.5 | 5.9
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=17362836
|Trait=Amyotrophic lateral sclerosis
|Title=Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data
|RiskAllele=
|Pval=0.0000090000000000000002
|OR=1.00
|ORtxt=[0.80-1.40]
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs11099864
|overall_frequency_n=62
|overall_frequency_d=128
|overall_frequency=0.484375
|n_genomes=37
|n_genomes_annotated=0
|n_haplomes=50
|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}}