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rs2270744

From SNPedia

Orientationminus
Stabilizedminus
Make rs2270744(C;C)
Make rs2270744(C;G)
Make rs2270744(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position8490582
GeneMYH10
is asnp
is mentioned by
dbSNPrs2270744
ClinGenrs2270744
ebirs2270744
HLIrs2270744
Exacrs2270744
Varsomers2270744
Maprs2270744
PheGenIrs2270744
hapmaprs2270744
1000 genomesrs2270744
hgdprs2270744
ensemblrs2270744
gopubmedrs2270744
geneviewrs2270744
scholarrs2270744
googlers2270744
pharmgkbrs2270744
gwascentralrs2270744
openSNPrs2270744
23andMers2270744
23andMe allrs2270744
SNP Nexus

SNPshotrs2270744
SNPdbers2270744
MSV3drs2270744
GWAS Ctlgrs2270744
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 27506496OA-icon.png] A Functional Polymorphism (rs937283) in the MDM2 Promoter Region is Associated with Poor Prognosis of Retinoblastoma in Chinese Han Population.