{{Rsnum
|rsid=3803185
|Gene=ARL11
|Chromosome=13
|position=49630889
|Orientation=minus
|ReferenceAllele=T
|MissenseAllele=C
|GMAF=0.3081
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ARL11
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 21.5 | 64.6 | 13.8
| HCB | 66.7 | 31.1 | 2.2
| JPT | 59.1 | 36.4 | 4.5
| YRI | 77.8 | 22.2 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 66.7 | 31.1 | 2.2
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{Venter SNP
|rsid=3803185
|allele=C
|frequency=0.467
|uid=1103649222084
|type=homozygous_SNP
|hugo=ARL11
|ensembl gene=ENSG00000152213
|ensembl transcript=ENST00000282026
|sift=TOLERATED
|disease=Defects in ARL11 may be a cause of susceptibility to chronic lymphocytic leukemia (CLL) (MIM:151400).
}}

{{GET Evidence
|gene=ARL11
|aa_change=Cys148Arg
|aa_change_short=C148R
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs3803185
|overall_frequency_n=4133
|overall_frequency_d=10754
|overall_frequency=0.384322
|n_genomes=28
|n_genomes_annotated=0
|n_haplomes=33
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.153
|nblosum100=8
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}