{{Rsnum
|rsid=387907348
|Chromosome=14
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ACTN1
|position=68925641
|Gene_s=ACTN1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=14
|CLNACC=RCV000034869.27
|CLNALLE=1
|CLNDBN=Platelet-type bleeding disorder 15
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN169278:615193:140957
|CLNHGVS=NC_000014.8:g.69392358C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=102575.0004
|Disease=Platelet-type bleeding disorder 15
|FwdALT=A
|FwdREF=G
|REF=C
|RSPOS=69392358
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907348
|GENEINFO=ACTN1:87
|GENE_ID=87
|GENE_NAME=ACTN1
}}