{{Rsnum
|rsid=35077384
|Gene=ZFYVE27
|Chromosome=10
|position=97749494
|Orientation=minus
|GMAF=0.02204
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=ZFYVE27
}}{{omim
|id=610244
|desc=SPASTIC PARAPLEGIA 33, AUTOSOMAL DOMINANT; SPG33
|rsnum=35077384
}}

{{omim
|id=610243
|desc=ZINC FINGER FYVE DOMAIN-CONTAINING PROTEIN 27; ZFYVE27
|rsnum=35077384
}}

{{ population diversity
| geno1 = (A;C)
| geno2 = (C;C)
| geno3 = 
| CEU | 1.7 | 98.3 | 0
| CHB | 0.0 | 100.0 | 0
| JPT | 2.2 | 97.8 | 0
| YRI | 13.3 | 86.7 | 0
}}
{{omim
|id=610243
|rsnum=35077384
|variant=0001
}}

{{ClinVar
|rsid=35077384
|Reversed=1
|FwdREF=C
|FwdALT=A
|REF=G
|ALT=T
|RSPOS=99509251
|CHROM=10
|GMAF=0.022
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050160000000150516110100
|GENEINFO=ZFYVE27:118813
|GENE_NAME=ZFYVE27
|GENE_ID=118813
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.99509251G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=610243.0001
|CLNSIG=5
|CLNCUI=C1853251
|CLNDBN=Spastic paraplegia 33, autosomal dominant
|Disease=Spastic paraplegia 33
|CLNACC=RCV000001352.1
|Tags=RV;PM;SLO;VLD;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.978; 0.02204
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1853251:610244
|COMMON=1
}}

{{GET Evidence
|gene=ZFYVE27
|aa_change=Gly191Val
|aa_change_short=G191V
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs35077384
|overall_frequency_n=326
|overall_frequency_d=10758
|overall_frequency=0.030303
|n_genomes=1
|n_genomes_annotated=0
|n_haplomes=1
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|in_omim=Y
|pph2_score=0.688
|genetests_testable=Y
|nblosum100=8
|autoscore=4
|webscore=N
|n_web_uneval=5
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}