{{Rsnum
|rsid=397518452
|Chromosome=12
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=HNRNPA1
|position=54283845
|Gene_s=HNRNPA1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=12
|CLNACC=RCV000055649.22
|CLNALLE=1
|CLNDBN=Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=CN180155:615424
|CLNHGVS=NC_000012.11:g.54677629A>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=164017.0001
|Disease=Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3
|FwdALT=T
|FwdREF=A
|GENEINFO=HNRNPA1:3178
|GENE_ID=3178
|GENE_NAME=HNRNPA1
|REF=A
|RSPOS=54677629
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=138
|rsid=397518452
}}