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rs1126772

From SNPedia

Orientationplus
Stabilizedplus
Make rs1126772(A;A)
Make rs1126772(A;G)
Make rs1126772(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position87983034
GeneSPP1
is asnp
is mentioned by
dbSNPrs1126772
dbSNP (classic)rs1126772
ClinGenrs1126772
ebirs1126772
HLIrs1126772
Exacrs1126772
Gnomadrs1126772
Varsomers1126772
LitVarrs1126772
Maprs1126772
PheGenIrs1126772
Biobankrs1126772
1000 genomesrs1126772
hgdprs1126772
ensemblrs1126772
geneviewrs1126772
scholarrs1126772
googlers1126772
pharmgkbrs1126772
gwascentralrs1126772
openSNPrs1126772
23andMers1126772
SNPshotrs1126772
SNPdbers1126772
MSV3drs1126772
GWAS Ctlgrs1126772
GMAF0.1878
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 22276228OA-icon.png] Polymorphism in Osteopontin Gene (SPP1) Is Associated with Asthma and Related Phenotypes in a Puerto Rican Population


[PMID 18335026OA-icon.png] Osteopontin and systemic lupus erythematosus association: a probable gene-gender interaction.


[PMID 19339987OA-icon.png] Age- and gender-specific modulation of serum osteopontin and interferon-alpha by osteopontin genotype in systemic lupus erythematosus.


[PMID 21513757] Behcet's disease exhibits an increased osteopontin serum level in active stage but no association with osteopontin and its receptor gene polymorphisms.


[PMID 23515922] Osteopontin in bone mineral density of very old Brazilians


[PMID 24084141] Investigation of Osteopontin Levels and Genomic Variation of Osteopontin 4 and Its Receptors in Type One Diabetes Mellitus


[PMID 24913806] Correlation between OPN gene polymorphisms and the risk of nasopharyngeal carcinoma


[PMID 25009318] Genetic association of osteopontin (OPN) and its receptor CD44 genes with susceptibility to Chinese gastric cancer patients


[PMID 25916533] [Relationship between osteopontin gene genetic polymorphisms and susceptibility of nasopharyngeal carcinoma in Guangxi Zhuang people]


[PMID 31036794OA-icon.png] The rs1126616 Single Nucleotide Polymorphism of the Osteopontin Gene Is Independently Associated with Cardiovascular Events in a Chronic Kidney Disease Cohort.


[PMID 33152124] Common gene variants within 3'-untranslated regions as modulators of multiple myeloma risk and survival.