{{Rsnum
|rsid=17166496
|Gene=FSTL4
|Chromosome=5
|position=133293192
|Orientation=plus
|GMAF=0.4568
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=FSTL4
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 34.5 | 47.8 | 17.7
| HCB | 13.9 | 32.8 | 53.3
| JPT | 10.6 | 42.5 | 46.9
| YRI | 12.9 | 47.6 | 39.5
| ASW | 19.3 | 42.1 | 38.6
| CHB | 13.9 | 32.8 | 53.3
| CHD | 8.5 | 39.6 | 51.9
| GIH | 18.8 | 57.4 | 23.8
| LWK | 15.5 | 49.1 | 35.5
| MEX | 25.9 | 46.6 | 27.6
| MKK | 15.4 | 49.4 | 35.3
| TSI | 38.2 | 49.0 | 12.7
| HapMapRevision=28
}}
[[rs17166496]] has been reported in a large study to be associated with [[type-1 diabetes]].

The risk allele (oriented to the dbSNP entry) is (C); the odds ratio associated with heterozygotes is 0.77 (CI 0.68-0.87), and for homozygotes, 1.09 (CI 0.92-1.29). {{PMID|17554300|OA=1
}}

Note: orientation of SNP is presumed correct but should be confirmed

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs17166496
|overall_frequency_n=58
|overall_frequency_d=128
|overall_frequency=0.453125
|n_genomes=38
|n_genomes_annotated=0
|n_haplomes=49
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}