{{Rsnum
|rsid=2306677
|Gene=ITPR2
|Chromosome=12
|position=26483453
|Orientation=minus
|GMAF=0.1901
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=ITPR2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 74.3 | 24.8 | 0.9
| HCB | 59.6 | 34.6 | 5.9
| JPT | 65.8 | 28.8 | 5.4
| YRI | 50.7 | 43.2 | 6.2
| ASW | 47.4 | 43.9 | 8.8
| CHB | 59.6 | 34.6 | 5.9
| CHD | 63.9 | 33.3 | 2.8
| GIH | 85.1 | 14.9 | 0.0
| LWK | 30.9 | 58.2 | 10.9
| MEX | 75.4 | 21.1 | 3.5
| MKK | 52.3 | 43.1 | 4.6
| TSI | 80.4 | 17.6 | 2.0
| HapMapRevision=28
}}

{{GWAS Summary
|SNP=rs2306677
|PubMedID=17827064
|Condition=Amyotrophic lateral sclerosis
|Gene=ITPR2
|Risk Allele=
|pValue=3.00E-006
|OR=1.58
|95CI=1.30-1.91
}}

{{PharmGKB
|RSID=rs2306677
|Name_s=
|Gene_s=ITPR2
|Feature=
|Evidence=PubMed ID:17827064; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS results: ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study (Initial Sample Size: 737 cases, 721 controls; Replication Sample Size: 1,030 cases, 1,195 controls). This variant is associated with Amyotrophic lateral sclerosis.
|Drugs=
|Drug Classes=
|Diseases=Amyotrophic Lateral Sclerosis
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA162356552
}}

{{PMID Auto
|PMID=19193627
|Title=A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis.
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2306677
|overall_frequency_n=99
|overall_frequency_d=128
|overall_frequency=0.773438
|n_genomes=51
|n_genomes_annotated=0
|n_haplomes=86
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|in_pharmgkb=Y
|autoscore=2
|webscore=N
}}

{{PMID Auto
|PMID=22795786
|Title=No association of five candidate genetic variants with amyotrophic lateral sclerosis in a Chinese population
}}

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