{{Rsnum
|rsid=74315450
|Chromosome=21
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=RUNX1
|position=34859485
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RUNX1
}}{{omim
|id=151385
|rsnum=74315450
|variant=0002
}}{{ClinVar
|rsid=74315450
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=36231782
|CHROM=21
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=RUNX1:861
|GENE_NAME=RUNX1
|GENE_ID=861
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000021.8:g.36231782C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=151385.0002
|CLNSIG=5
|CLNCUI=C1832388
|CLNDBN=Familial platelet disorder with associated myeloid malignancy
|Disease=Familial platelet disorder with associated myeloid malignancy
|CLNACC=RCV000015550.23
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1832388:601399:71290
}}