{{Rsnum
|rsid=6871748
|Chromosome=5
|position=35885880
|Orientation=plus
|GMAF=0.1938
|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 | 7.7 | 33.8 | 58.5
| HCB | 9.3 | 18.6 | 72.1
| JPT | 2.2 | 33.3 | 64.4
| YRI | 1.6 | 7.9 | 90.5
| ASW | 0.0 | 0.0 | 0.0
| CHB | 9.3 | 18.6 | 72.1
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{omim
|desc=MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO, 3; MS3
|id=612595
|rsnum=6871748
}}

{{PharmGKB
|RSID=rs6871748
|Name_s=
|Gene_s=-
|Feature=
|Evidence=PubMed ID:17660816
|Annotation=In a case-control study of Nordic populations, rs6871748 was associated with risk of multiple sclerosis.
|Drugs=
|Drug Classes=
|Diseases=Multiple Sclerosis
|Curation Level=Curated
|PharmGKB Accession ID=PA162356129
}}

{{PMID Auto
|PMID=19221116
|Title=Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS.
|OA=1
}}

{{GET Evidence
|impact=pharmacogenetic
|qualified_impact=Insufficiently evaluated pharmacogenetic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs6871748
|overall_frequency_n=23
|overall_frequency_d=126
|overall_frequency=0.18254
|n_genomes=15
|n_genomes_annotated=0
|n_haplomes=16
|n_articles=1
|n_articles_annotated=0
|in_pharmgkb=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}