{{Rsnum
|rsid=387907172
|Chromosome=16
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FA2H
|position=74719067
|Gene_s=FA2H
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=16
|CLNACC=RCV000024321.2
|CLNALLE=1
|CLNDBN=Spastic paraplegia 35
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK56080:C2676236:612319:171629
|CLNHGVS=NC_000016.9:g.74752965A>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=611026.0007
|Disease=Spastic paraplegia 35
|FwdALT=C
|FwdREF=T
|REF=A
|RSPOS=74752965
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907172
|GENEINFO=FA2H:79152
|GENE_ID=79152
|GENE_NAME=FA2H
}}