{{Rsnum
|rsid=121912498
|Chromosome=21
|position=34886866
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=RUNX1
|Gene_s=RUNX1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=151385
|rsnum=121912498
|variant=0003
}}{{ClinVar
|rsid=121912498
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=36259163
|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.36259163T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=151385.0003
|CLNSIG=5
|CLNCUI=C1832388
|CLNDBN=Familial platelet disorder with associated myeloid malignancy
|Disease=Familial platelet disorder with associated myeloid malignancy
|CLNACC=RCV000015551.23
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1832388:601399:71290
}}