{{Rsnum
|rsid=682632
|Gene=TEK
|Chromosome=9
|position=27183465
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=A
|GMAF=0.01607
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=TEK
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 92.0 | 8.0 | 0.0
| HCB | 99.3 | 0.7 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 99.3 | 0.7 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 97.0 | 3.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 98.3 | 1.7 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 97.0 | 2.0 | 1.0
| HapMapRevision=28
}}{{Venter SNP
|rsid=682632
|allele=C
|frequency=0.967
|uid=1103652056586
|type=homozygous_SNP
|hugo=TEK
|ensembl gene=ENSG00000120156
|ensembl transcript=ENST00000346448
|sift=TOLERATED
|disease=Defects in TEK are a cause of dominantly inherited venous malformations (VMCM) (MIM:600195); an error of vascular morphogenesis characterized by dilated, serpiginous channels.
}}

{{GET Evidence
|gene=TEK
|aa_change=Gln346Pro
|aa_change_short=Q346P
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs682632
|overall_frequency_n=10467
|overall_frequency_d=10758
|overall_frequency=0.97295
|n_genomes=56
|n_genomes_annotated=0
|n_haplomes=108
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|genetests_reviewed=Y
|nblosum100=4
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}