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rs6747096

From SNPedia

Merged intors12457
Orientationminus
Stabilizedplus
Make rs6747096(A;A)
Make rs6747096(A;G)
Make rs6747096(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position223998125
GeneSERPINE2
is asnp
is mentioned by
dbSNPrs6747096
ebirs6747096
HLIrs6747096
Exacrs6747096
Varsomers6747096
Maprs6747096
PheGenIrs6747096
hapmaprs6747096
1000 genomesrs6747096
hgdprs6747096
ensemblrs6747096
gopubmedrs6747096
geneviewrs6747096
scholarrs6747096
googlers6747096
pharmgkbrs6747096
gwascentralrs6747096
openSNPrs6747096
23andMers6747096
23andMe allrs6747096
SNP Nexus

SNPshotrs6747096
SNPdbers6747096
MSV3drs6747096
GWAS Ctlgrs6747096
StatusMerged into rs12457
GMAF0.2459
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 19604412OA-icon.png] Absence of association between SERPINE2 genetic polymorphisms and chronic obstructive pulmonary disease in Han Chinese: a case-control cohort study


[PMID 19626039] Lack of replication of celiac disease risk variants reported in a Spanish population using an independent Spanish sample

[PMID 16358219OA-icon.png] The SERPINE2 gene is associated with chronic obstructive pulmonary disease.

[PMID 16773582OA-icon.png] The SERPINE2 gene and chronic obstructive pulmonary disease.

[PMID 18241860] Combined functional and positional gene information for the identification of susceptibility variants in celiac disease.

[PMID 18471539OA-icon.png] No evidence in a large UK collection for celiac disease risk variants reported by a Spanish study.

[PMID 19949669OA-icon.png] SERPINE2 polymorphisms and chronic obstructive pulmonary disease.

[PMID 20233420OA-icon.png] Cluster analysis in severe emphysema subjects using phenotype and genotype data: an exploratory investigation.