{{Rsnum
|rsid=17292650
|Gene=MPL
|Chromosome=1
|position=43338136
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=T
|GMAF=0.01148
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=MPL
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 99.1 | 0.9 | 0.0
| HCB | 98.5 | 1.5 | 0.0
| JPT | 0.0 | 0.0 | 0.0
| YRI | 92.5 | 6.2 | 1.4
| ASW | 86.0 | 14.0 | 0.0
| CHB | 98.5 | 1.5 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 93.6 | 6.4 | 0.0
| MEX | 96.6 | 3.4 | 0.0
| MKK | 95.5 | 4.5 | 0.0
| TSI | 99.0 | 1.0 | 0.0
| HapMapRevision=28
}}{{omim
|desc=THROMBOCYTOSIS, SUSCEPTIBILITY TO
|id=159530
|rsnum=17292650
|variant=0009
}}

{{ neighbor
| rsid = 28928907
| distance = 498
}}

{{ClinVar
|rsid=17292650
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=43338136
|CHROM=1
|GMAF=0.0114
|dbSNPBuildID=123
|SSR=0
|SAO=1
|VP=0x050360000a05150517110100
|GENEINFO=MPL:4352
|GENE_NAME=MPL
|GENE_ID=4352
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.43338136G>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_005373.2:c.117G>T; 159530.0009
|CLNSIG=255
|CLNCUI=C1865987
|CLNDBN=Thrombocytosis, benign familial microcytic; AllHighlyPenetrant
|Disease=Thrombocytosis; AllHighlyPenetrant
|CLNACC=RCV000015225.1; RCV000121535.1
|Tags=PM;S3D;SLO;NSM;REF;ASP;VLD;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.9885; 0.01148
|CLNDSDB=MedGen:OMIM:Orphanet; MedGen
|CLNDSDBID=C1865987:601977:ORPHA3318; CN169374
|COMMON=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}