{{Rsnum
|rsid=17855765
|Gene=SLC39A4
|Chromosome=8
|position=144415944
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.4348
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=SLC39A4
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 30.8 | 44.6 | 24.6
| HCB | 28.9 | 51.1 | 20.0
| JPT | 40.9 | 45.5 | 13.6
| YRI | 58.7 | 33.3 | 7.9
| ASW | 0.0 | 0.0 | 0.0
| CHB | 28.9 | 51.1 | 20.0
| 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=17855765
|allele=T
|frequency=0.467
|uid=1103652472440
|type=homozygous_SNP
|hugo=SLC39A4
|ensembl gene=ENSG00000147804
|ensembl transcript=ENST00000301305
|sift=
|disease=Defects in SLC39A4 are the cause of acrodermatitis enteropathica zinc-deficiency type (AEZ) (MIM:201100). AEZ is a rare autosomal recessive disease caused by the inability to absorb sufficient zinc. The clinicals features are growth retardation, immune-system dysfunction, alopecia, severe dermatitis, diarrhea and occasionally mental disorders.
}}

{{ neighbor
| rsid = 2977838
| distance = 917
}}
{{ neighbor
| rsid = 2280838
| distance = 674
}}

{{GET Evidence
|gene=SLC39A4
|aa_change=Ala114Thr
|aa_change_short=A114T
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs17855765
|overall_frequency_n=4610
|overall_frequency_d=10648
|overall_frequency=0.432945
|n_genomes=33
|n_genomes_annotated=0
|n_haplomes=40
|n_articles=0
|n_articles_annotated=0
|nblosum100=1
|autoscore=0
|webscore=N
}}
{{on chip | HumanOmni1Quad}}