{{Rsnum
|rsid=117767867
|Gene=SLC16A11
|Chromosome=17
|position=7043011
|Orientation=plus
|GMAF=0.07071
|Gene_s=SLC16A11
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}[[rs117767867]] is a SNP in the [[SLC16A11]] gene on chromosome 17. 

This SNP, [[rs117767867]] is considered the tag SNP for a haplotype consisting of 4 missense variants identified as relatively common in the Native American population and having introgressed into modern humans via admixture with Neanderthals. The other 3 missense variants are [[rs13342692]], [[rs75418188]], and [[rs75493593]]. This haplotype raises the risk by 25% in heterozygotes and 50% in homozygotes for [[type-2 diabetes]], and it may also lead to the development of [[type-2 diabetes]] at a younger age and lower BMI. This haplotype is found at ~50% frequency in Native American samples and ~10% in east Asian, but is rare in Europeans and Africans.{{doi|10.1038/nature12828}}