{{Rsnum
|rsid=11190870
|Chromosome=10
|position=102979207
|Orientation=plus
|GMAF=0.4238
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=132
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 15.9 | 42.5 | 41.6
| HCB | 24.8 | 48.9 | 26.3
| JPT | 17.7 | 56.6 | 25.7
| YRI | 11.6 | 44.2 | 44.2
| ASW | 15.8 | 40.4 | 43.9
| CHB | 24.8 | 48.9 | 26.3
| CHD | 22.9 | 49.5 | 27.5
| GIH | 3.0 | 42.6 | 54.5
| LWK | 20.0 | 48.2 | 31.8
| MEX | 13.8 | 36.2 | 50.0
| MKK | 19.2 | 48.1 | 32.7
| TSI | 13.7 | 49.0 | 37.3
| HapMapRevision=28
}}{{PMID Auto
|PMID=21331621
|Title=Genetic variants in ultraconserved elements and risk of breast cancer in Chinese population
}}

The T allele of this SNP is associated with an increased risk of [[scoliosis]] in adolescent Japanese girls. [http://www.nature.com/ng/journal/v43/n12/full/ng.974.html]

{{PMID Auto GWAS
|PMID=22019779
|Trait=None
|Title=A genome-wide association study identifies common variants near LBX1 associated with adolescent idiopathic scoliosis.
|RiskAllele=
|Pval=1E-19
|OR=1.5600
|ORtxt=None
}}

{{PMID Auto
|PMID=23096252
|Title=Association of rs11190870 near LBX1 with adolescent idiopathic scoliosis susceptibility in a Han Chinese population.
|OA=1
}}

{{PMID Auto
|PMID=24878781
|Title=Association of rs11190870 near LBX1 with adolescent idiopathic scoliosis in East Asians: a systematic review and meta-analysis
}}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}