{{Rsnum
|rsid=1062087
|Gene=TBC1D4
|Chromosome=13
|position=75310080
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.2815
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=TBC1D4
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 82.3 | 15.9 | 1.8
| HCB | 62.8 | 35.0 | 2.2
| JPT | 55.8 | 34.5 | 9.7
| YRI | 12.9 | 46.9 | 40.1
| ASW | 28.1 | 59.6 | 12.3
| CHB | 62.8 | 35.0 | 2.2
| CHD | 68.8 | 30.3 | 0.9
| GIH | 87.1 | 12.9 | 0.0
| LWK | 20.0 | 51.8 | 28.2
| MEX | 60.3 | 34.5 | 5.2
| MKK | 23.1 | 47.4 | 29.5
| TSI | 72.5 | 25.5 | 2.0
| HapMapRevision=28
}}

{{Venter SNP
|rsid=1062087
|allele=T
|frequency=0.925
|uid=1103649268365
|type=homozygous_SNP
|hugo=TBC1D4
|ensembl gene=ENSG00000136111
|ensembl transcript=ENST00000377636
|sift=TOLERATED
|disease=May be involved in atopic dermatitis (AD).
}}

{{GET Evidence
|gene=TBC1D4
|aa_change=Val819Ile
|aa_change_short=V819I
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1062087
|overall_frequency_n=7379
|overall_frequency_d=9624
|overall_frequency=0.766729
|n_genomes=50
|n_genomes_annotated=0
|n_haplomes=85
|n_articles=0
|n_articles_annotated=0
|nblosum100=-4
|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}}