{{Rsnum
|rsid=1671021
|Gene=LLGL2
|Chromosome=17
|position=75569090
|Orientation=minus
|GMAF=0.449
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=LLGL2
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 41.6 | 42.5 | 15.9
| HCB | 60.6 | 35.0 | 4.4
| JPT | 72.6 | 23.9 | 3.5
| YRI | 0.7 | 17.1 | 82.2
| ASW | 5.3 | 28.1 | 66.7
| CHB | 60.6 | 35.0 | 4.4
| CHD | 66.1 | 30.3 | 3.7
| GIH | 45.5 | 50.5 | 4.0
| LWK | 0.0 | 11.0 | 89.0
| MEX | 44.8 | 43.1 | 12.1
| MKK | 5.8 | 26.3 | 67.9
| TSI | 33.3 | 51.0 | 15.7
| 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
}}

{{GET Evidence
|gene=LLGL2
|aa_change=Phe479Leu
|aa_change_short=F479L
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1671021
|overall_frequency_n=5780
|overall_frequency_d=10754
|overall_frequency=0.537474
|n_genomes=41
|n_genomes_annotated=0
|n_haplomes=62
|n_articles=0
|n_articles_annotated=0
|nblosum100=0
|autoscore=0
|webscore=N
}}

{{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}}