{{Rsnum
|rsid=387907264
|Chromosome=17
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=PFN1
|position=4946742
|Gene_s=PFN1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=17
|CLNACC=RCV000030694.23
|CLNALLE=1
|CLNDBN=Amyotrophic lateral sclerosis 18
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1450:CN143708:614808:803
|CLNHGVS=NC_000017.10:g.4850037A>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=176610.0001
|Disease=Amyotrophic lateral sclerosis 18
|FwdALT=G
|FwdREF=T
|REF=A
|RSPOS=4850037
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907264
|GENEINFO=PFN1:5216
|GENE_ID=5216
|GENE_NAME=PFN1
}}