{{Rsnum
|rsid=9527025
|Gene=KL
|Chromosome=13
|position=33054056
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=C
|GMAF=0.1304
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Summary=intelligence; longevity
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=KL
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 1.5 | 29.2 | 69.2
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 1.6 | 38.1 | 60.3
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 0.0 | 100.0
| 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=9527025
|allele=C
|frequency=0.175
|uid=1103649192250
|type=heterozygous_SNP
|hugo=KL
|ensembl gene=ENSG00000133116
|ensembl transcript=ENST00000255481
|sift=TOLERATED
|disease=Defects in KL may be a cause of chronic renal failure complications.
}}

{{ neighbor
| rsid = 9536314
| distance = 55
}}{{PMID Auto
|PMID=18818748
|Title=Preterm birth in Caucasians is associated with coagulation and inflammation pathway gene variants.
|OA=1
}}

{{PMID Auto
|PMID=20401335
|Title=Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.
|OA=1
}}{{GET Evidence
|gene=KL
|aa_change=Cys370Ser
|aa_change_short=C370S
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs9527025
|overall_frequency_n=1830
|overall_frequency_d=10758
|overall_frequency=0.170106
|n_genomes=14
|n_genomes_annotated=0
|n_haplomes=17
|n_articles=0
|n_articles_annotated=0
|nblosum100=3
|autoscore=0
|webscore=N
}}