{{Rsnum
|rsid=140547520
|Gene=PFN1
|Chromosome=17
|position=4945973
|Orientation=plus
|GMAF=0.0004591
|Gene_s=PFN1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ClinVar
|ALT=C
|CAF=0.9995; 0.0004591
|CHROM=17
|CLNACC=RCV000030697.23
|CLNALLE=1
|CLNDBN=Amyotrophic lateral sclerosis 18
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1450:CN143708:614808:803
|CLNHGVS=NC_000017.10:g.4849268T>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=176610.0004
|COMMON=0
|Disease=Amyotrophic lateral sclerosis 18
|FwdALT=C
|FwdREF=T
|GENEINFO=PFN1:5216
|GENE_ID=5216
|GENE_NAME=PFN1
|REF=T
|RSPOS=4849268
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000040016110100
|WGT=0
|dbSNPBuildID=134
|rsid=140547520
}}