{{Rsnum
|rsid=121918217
|Chromosome=16
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=FA2H
|position=74774653
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FA2H
}}{{omim
|id=611026
|rsnum=121918217
|variant=0002
}}{{ClinVar
|rsid=121918217
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=74808551
|CHROM=16
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=FA2H:79152
|GENE_NAME=FA2H
|GENE_ID=79152
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.74808551C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=611026.0002
|CLNSIG=5
|CLNCUI=C2676236
|CLNDBN=Spastic paraplegia 35
|Disease=Spastic paraplegia 35
|CLNACC=RCV000001099.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK56080:C2676236:612319:171629
}}