{{Rsnum
|rsid=6007897
|Gene=CELSR1
|Chromosome=22
|position=46384624
|Orientation=plus
|GMAF=0.2227
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=CELSR1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 1.8 | 31.5 | 66.7
| HCB | 0.0 | 2.9 | 97.1
| JPT | 0.0 | 2.7 | 97.3
| YRI | 37.8 | 53.8 | 8.4
| ASW | 29.1 | 58.2 | 12.7
| CHB | 0.0 | 2.9 | 97.1
| CHD | 0.0 | 0.9 | 99.1
| GIH | 0.0 | 11.9 | 88.1
| LWK | 40.7 | 45.4 | 13.9
| MEX | 0.0 | 13.8 | 86.2
| MKK | 20.6 | 53.5 | 25.8
| TSI | 5.9 | 29.7 | 64.4
| HapMapRevision=28
}}{{PMID Auto
|PMID=19403135
|Title=Identification of CELSR1 as a susceptibility gene for ischemic stroke in Japanese individuals by a genome-wide association study
}}

{{PMID Auto
|PMID=18454203
|Title=Differential allelic expression in the human genome: a robust approach to identify genetic and epigenetic cis-acting mechanisms regulating gene expression.
|OA=1
}}

{{GET Evidence
|gene=CELSR1
|aa_change=Thr2268Ala
|aa_change_short=T2268A
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs6007897
|overall_frequency_n=3238
|overall_frequency_d=10758
|overall_frequency=0.300985
|n_genomes=32
|n_genomes_annotated=0
|n_haplomes=39
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.009
|nblosum100=1
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}