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rs1045411

From SNPedia

Orientationminus
Stabilizedminus
Make rs1045411(A;A)
Make rs1045411(A;G)
Make rs1045411(G;G)
ReferenceGRCh38 38.1/142
Chromosome13
Position30459095
GeneHMGB1
is asnp
is mentioned by
dbSNPrs1045411
ebirs1045411
HLIrs1045411
Exacrs1045411
Varsomers1045411
Maprs1045411
PheGenIrs1045411
hapmaprs1045411
1000 genomesrs1045411
hgdprs1045411
ensemblrs1045411
gopubmedrs1045411
geneviewrs1045411
scholarrs1045411
googlers1045411
pharmgkbrs1045411
gwascentralrs1045411
openSNPrs1045411
23andMers1045411
23andMe allrs1045411
SNP Nexus

SNPshotrs1045411
SNPdbers1045411
MSV3drs1045411
GWAS Ctlgrs1045411
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 25639284] HMGB1 Genetic Polymorphisms in Oral Squamous Cell Carcinoma and Oral Lichen Planus Patients


[PMID 27076788] Effects of HMGB1 Polymorphisms on the Susceptibility and Progression of Hepatocellular Carcinoma


[PMID 27665685] Association of HMGB1 Gene Polymorphisms with Risk of Colorectal Cancer in a Chinese Population.