{{Rsnum
|rsid=121908288
|Gene=FIG4
|Chromosome=6
|position=109735199
|Orientation=plus
|GMAF=0.0009183
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=FIG4
}}{{omim
|id=609390
|rsnum=121908288
|variant=0003
}}
{{omim
|id=609390
|rsnum=121908288
|variant=0006
}}{{ClinVar
|rsid=121908288
|Reversed=0
|FwdREF=C
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=110056402
|CHROM=6
|GMAF=0.0009
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000016110100
|GENEINFO=FIG4:9896
|GENE_NAME=FIG4
|GENE_ID=9896
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000006.11:g.110056402C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=609390.0003; 609390.0006
|CLNSIG=5
|CLNCUI=C1970011
|CLNDBN=Charcot-Marie-Tooth disease, type 4J; Amyotrophic lateral sclerosis type 11
|Disease=Charcot-Marie-Tooth disease; Amyotrophic lateral sclerosis type 11
|CLNACC=RCV000001793.1; RCV000001796.1
|Tags=PM;S3D;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9991; 0.0009183; .
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1468:C1970011:611228:139515; NBK1450:C2675491:612577:803
|COMMON=1
}}