{{Rsnum
|rsid=121913119
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=FH
|position=241504066
|Gene_s=FH
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=136850
|rsnum=121913119
|variant=0002
}}{{ClinVar
|rsid=121913119
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=241504066
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000a05000002110100
|GENEINFO=FH:2271
|GENE_NAME=FH
|GENE_ID=2271
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.241504066C>G
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000143.3:c.1084G>C; 136850.0002
|CLNSIG=5
|CLNCUI=C0342770
|CLNDBN=Fumarase deficiency
|Disease=Fumarase deficiency
|CLNACC=RCV000017618.26
|Tags=RV;PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1506:C0342770:606812:ORPHA24:237983002
}}