{{Rsnum
|rsid=121912499
|Chromosome=21
|position=34799407
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=RUNX1
|Gene_s=RUNX1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=151385
|rsnum=121912499
|variant=0005
}}{{ClinVar
|rsid=121912499
|Reversed=1
|FwdREF=C
|FwdALT=A
|REF=G
|ALT=T
|RSPOS=36171704
|CHROM=21
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=RUNX1:861
|GENE_NAME=RUNX1
|GENE_ID=861
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000021.8:g.36171704G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=151385.0005
|CLNSIG=5
|CLNCUI=C1832388
|CLNDBN=Familial platelet disorder with associated myeloid malignancy
|Disease=Familial platelet disorder with associated myeloid malignancy
|CLNACC=RCV000015553.21
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1832388:601399:71290
}}