{{Rsnum
|rsid=11172113
|Gene=LRP1
|Chromosome=12
|position=57133500
|Orientation=plus
|GMAF=0.3898
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=LRP1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 12.4 | 48.7 | 38.9
| HCB | 8.8 | 32.8 | 58.4
| JPT | 2.7 | 31.9 | 65.5
| YRI | 20.4 | 57.1 | 22.4
| ASW | 14.0 | 50.9 | 35.1
| CHB | 8.8 | 32.8 | 58.4
| CHD | 6.4 | 40.4 | 53.2
| GIH | 16.8 | 45.5 | 37.6
| LWK | 17.3 | 51.8 | 30.9
| MEX | 20.7 | 53.4 | 25.9
| MKK | 11.6 | 51.0 | 37.4
| TSI | 11.8 | 49.0 | 39.2
| HapMapRevision=28
}}[[rs11172113]] is a SNP on ch 12q13.3 in the [[LRP1]] gene.

A large GWAS study of over 5,000 patients with [[migraines]] and a meta-analysis concluded that this SNP was one of three influencing the condition, albeit with only slight risk changes on its own. The odds ratio for the less common [[rs11172113]](C) allele was 0.9 (CI: 0.87 - 0.93, p = 4.3 x 10e-9).{{doi|10.1038/ng.856}}

{{PMID Auto GWAS
|PMID=21666692
|Trait=None
|Title=Genome-wide association study reveals three susceptibility loci for common migraine in the general population.
|RiskAllele=T
|Pval=4E-9
|OR=1.1100
|ORtxt=[1.08-1.15]
|OA=1
}}

{{PMID Auto
|PMID=22072275
|Title=Genetics of migraine in the age of genome-wide association studies
|OA=1
}}

{{PMID Auto GWAS
|PMID=21946350
|Trait=None
|Title=Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.
|RiskAllele=T
|Pval=1E-8
|OR=0.0320
|ORtxt=[0.020-0.044] unit decrease
|OA=1
}}

{{PMID Auto GWAS
|PMID=22683712
|Trait=None
|Title=Genome-wide association analysis identifies susceptibility loci for migraine without aura.
|RiskAllele=
|Pval=3E-8
|OR=1.1600
|ORtxt=None
|OA=1
}}

{{PMID Auto GWAS
  |PMID=23284291
  |Trait=Pulmonary function (interaction)
  |Title=Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.
  |RiskAllele=
  |Pval=8E-6
  |OR=NR
  |ORtxt=NR
  |OA=1
}}

{{PMID Auto
|PMID=24021092
|Title=PRDM16 rs2651899 Variant Is a Risk Factor for Chinese Common Migraine Patients
}}

{{PMID Auto
|PMID=23294458
|Title=Replication and meta-analysis of common variants identifies a genome-wide significant locus in migraine
}}

{{PMID Auto GWAS
  |PMID=23793025
  |Trait=Migraine
  |Title=Genome-wide meta-analysis identifies new susceptibility loci for migraine.
  |RiskAllele=
  |Pval=4E-19
  |OR=1.11
  |ORtxt=[1.09-1.14]
  }}

{{PMID Auto
|PMID=24674449
|Title=A replication study of GWAS findings in migraine identifies association in a Swedish case-control sample
|OA=1
}}

{{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}}