{{Rsnum
|rsid=7076156
|Gene=ZNF365
|Chromosome=10
|position=62655424
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=G
|GMAF=0.152
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ZNF365
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 5.3 | 33.6 | 61.1
| HCB | 0.7 | 14.6 | 84.7
| JPT | 0.9 | 13.3 | 85.8
| YRI | 0.0 | 0.7 | 99.3
| ASW | 1.8 | 12.3 | 86.0
| CHB | 0.7 | 14.6 | 84.7
| CHD | 0.0 | 9.3 | 90.7
| GIH | 3.0 | 25.7 | 71.3
| LWK | 0.0 | 3.6 | 96.4
| MEX | 1.7 | 19.0 | 79.3
| MKK | 0.6 | 25.6 | 73.7
| TSI | 4.9 | 40.2 | 54.9
| HapMapRevision=28
}}{{PMID Auto
|PMID=21257989
|Title=Variants in ZNF365 isoform D are associated with Crohn's disease
|OA=1
}}

{{omim
|desc=URIC ACID NEPHROLITHIASIS, SUSCEPTIBILITY TO
|id=607818
|rsnum=7076156
|variant=0001
}}

{{Venter SNP
|rsid=7076156
|allele=G
|frequency=0.792
|uid=1103649958175
|type=homozygous_SNP
|hugo=ZNF365
|ensembl gene=ENSG00000138311
|ensembl transcript=ENST00000344640
|sift=
|disease=Defects in ZNF365 may be a cause of susceptibility to uric acid nephrolithiasis (UAN) (MIM:605990). UAN occurs when the urine becomes overly concentrated with uric acid that may form small crystals.
}}

{{PMID Auto GWAS
|PMID=22412388
|Trait=None
|Title=A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.
|RiskAllele=G
|Pval=7E-9
|OR=1.1900
|ORtxt=None
|OA=1
}}

{{ClinVar
|rsid=7076156
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=64415184
|CHROM=10
|GMAF=0.1516
|dbSNPBuildID=116
|SSR=0
|SAO=1
|VP=0x05016800000015051f130100
|GENEINFO=ZNF365:22891
|GENE_NAME=ZNF365
|GENE_ID=22891
|WGT=0
|VC=SNV
|CLNALLE=0
|CLNHGVS=NC_000010.10:g.64415184A\x3d
|CLNORIGIN=1
|CLNSRCID=
607818.0001
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000002951.1
|Tags=PM;PMC;SLO;VLD;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD;MTP;OM
|CAF=0.152; 0.848
|CLNDBN=Uric acid nephrolithiasis, susceptibility to
|CLNSRC=OMIM Allelic Variant
|COMMON=1
|Disease=Uric acid nephrolithiasis
}}

{{GET Evidence
|gene=ZNF365
|aa_change=Thr62Ala
|aa_change_short=T62A
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs7076156
|n_genomes=1
|n_genomes_annotated=0
|n_haplomes=1
|n_articles=0
|n_articles_annotated=0
|nblosum100=1
|autoscore=1
|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}}