{{Rsnum
|rsid=1755289
|Chromosome=9
|position=17938353
|Orientation=plus
|GMAF=0.4399
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 37.2 | 48.7 | 14.2
| HCB | 34.3 | 50.0 | 15.7
| JPT | 42.0 | 41.1 | 17.0
| YRI | 9.5 | 38.8 | 51.7
| ASW | 14.0 | 47.4 | 38.6
| CHB | 34.3 | 50.0 | 15.7
| CHD | 30.2 | 48.1 | 21.7
| GIH | 28.7 | 52.5 | 18.8
| LWK | 7.3 | 32.1 | 60.6
| MEX | 43.1 | 51.7 | 5.2
| MKK | 12.2 | 38.5 | 49.4
| TSI | 41.2 | 48.0 | 10.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19010793
|Trait=Multiple sclerosis
|Title=Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
|RiskAllele=
|Pval=0.000003
|OR=1.35
|ORtxt=[NR]
}}

{{PharmGKB
|RSID=rs1755289
|Name_s=
|Gene_s=-
|Feature=
|Evidence=PubMed ID:19010793; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS results: Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. (Initial Sample Size: 978 cases, 883 controls; Replication Sample Size: NR); (Region: 9p22.2; Reported Gene(s): SH3GL2; Risk Allele: rs1755289-?); (p-value= 0.000003).This variant is associated with Multiple sclerosis.
|Drugs=
|Drug Classes=
|Diseases=Multiple Sclerosis
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA164740711
}}

{{PMID Auto
|PMID=20944657
|Title=Replication of top markers of a genome-wide association study in multiple sclerosis in Spain.
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1755289
|overall_frequency_n=66
|overall_frequency_d=128
|overall_frequency=0.515625
|n_genomes=40
|n_genomes_annotated=0
|n_haplomes=56
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|in_pharmgkb=Y
|autoscore=2
|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}}