{{Rsnum
|rsid=766420
|Gene=TKTL1
|Chromosome=X
|position=154326058
|Orientation=minus
|GMAF=0.3071
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=TKTL1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 15.2 | 16.1 | 68.8
| HCB | 8.0 | 14.6 | 77.4
| JPT | 12.5 | 12.5 | 75.0
| YRI | 60.0 | 22.1 | 17.9
| ASW | 28.1 | 28.1 | 43.9
| CHB | 8.0 | 14.6 | 77.4
| CHD | 12.8 | 16.5 | 70.6
| GIH | 32.7 | 16.8 | 50.5
| LWK | 52.3 | 24.8 | 22.9
| MEX | 10.3 | 15.5 | 74.1
| MKK | 47.7 | 23.9 | 28.4
| TSI | 11.1 | 19.2 | 69.7
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=19419973
|Trait=Bilirubin levels
|Title=Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia
|RiskAllele=G
|Pval=9E-9
|OR=0.18
|ORtxt=[0.12-0.24] SD decrease
|OA=1
}}

{{PharmGKB
|RSID=rs766420
|Name_s=
|Gene_s=TKTL1
|Feature=
|Evidence=PubMed ID:19419973
|Annotation=This variant is on the X chromosome near the G6PD (glucose-6-phosphatedehydrogenase) gene and associated with serum bilirubin levels in a genome wide association scan from 4300 Sardinian individuals.
|Drugs=
|Drug Classes=
|Diseases=Hyperbilirubinemia
|Curation Level=Curated
|PharmGKB Accession ID=PA164758020
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs766420
|overall_frequency_n=32
|overall_frequency_d=92
|overall_frequency=0.347826
|n_genomes=21
|n_genomes_annotated=0
|n_haplomes=36
|n_articles=1
|n_articles_annotated=0
|in_gwas=Y
|in_pharmgkb=Y
|autoscore=2
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}