{{Rsnum
|rsid=3733242
|Gene=SHROOM3
|Chromosome=4
|position=76754352
|Orientation=minus
|GMAF=0.4876
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=SHROOM3
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 9.7 | 59.3 | 31.0
| HCB | 27.9 | 50.7 | 21.3
| JPT | 23.9 | 54.9 | 21.2
| YRI | 52.4 | 33.3 | 14.3
| ASW | 54.4 | 29.8 | 15.8
| CHB | 27.9 | 50.7 | 21.3
| CHD | 30.3 | 48.6 | 21.1
| GIH | 32.0 | 42.0 | 26.0
| LWK | 53.6 | 40.0 | 6.4
| MEX | 24.1 | 43.1 | 32.8
| MKK | 29.5 | 51.3 | 19.2
| TSI | 7.8 | 41.2 | 51.0
| HapMapRevision=28
}}
{{PMID Auto
|PMID=19740415
|Title=Genome-wide association reveals three SNPs associated with sporadic amyotrophic lateral sclerosis through a two-locus analysis
|OA=1
}}

{{PMID Auto
|PMID=17362836
|Title=Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data.
}}

{{GET Evidence
|gene=SHROOM3
|aa_change=Pro1289Leu
|aa_change_short=P1289L
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs3733242
|overall_frequency_n=60
|overall_frequency_d=128
|overall_frequency=0.46875
|n_genomes=31
|n_genomes_annotated=0
|n_haplomes=47
|n_articles=0
|n_articles_annotated=0
|nblosum100=7
|autoscore=0
|webscore=N
}}

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