rs1045411

Orientation

minus

Stabilized

minus

Make rs1045411(A;A)

Make rs1045411(A;G)

Make rs1045411(G;G)

Reference

GRCh38 38.1/142

Chromosome

13

Position

30459095

Gene

HMGB1

is a	snp
is	mentioned by
dbSNP	rs1045411
dbSNP (classic)	rs1045411
ClinGen	rs1045411
ebi	rs1045411
HLI	rs1045411
Exac	rs1045411
Gnomad	rs1045411
Varsome	rs1045411
LitVar	rs1045411
Map	rs1045411
PheGenI	rs1045411
Biobank	rs1045411
1000 genomes	rs1045411
hgdp	rs1045411
ensembl	rs1045411
geneview	rs1045411
scholar	rs1045411
google	rs1045411
pharmgkb	rs1045411
gwascentral	rs1045411
openSNP	rs1045411
23andMe	rs1045411
23andMe all	rs1045411
SNPshot	rs1045411
SNPdbe	rs1045411
MSV3d	rs1045411
GWAS Ctlg	rs1045411

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.

[PMID 29104475] Association of HMGB1 Gene Polymorphisms with Lung Cancer Susceptibility and Clinical Aspects.

[PMID 30423384] Associations between HMGB1 gene polymorphisms and susceptibility and clinical outcomes in Chinese Han sepsis patients.

[PMID 30562142] Association of High Mobility Group Box Protein B1 Gene Polymorphisms with Pneumonia Susceptibility and Severity.