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rs11226613

From SNPedia

Orientationplus
Stabilizedplus
Make rs11226613(A;A)
Make rs11226613(A;T)
Make rs11226613(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position105101791
GeneCARD17
is asnp
is mentioned by
dbSNPrs11226613
ebirs11226613
HLIrs11226613
Exacrs11226613
Varsomers11226613
Maprs11226613
PheGenIrs11226613
hapmaprs11226613
1000 genomesrs11226613
hgdprs11226613
ensemblrs11226613
gopubmedrs11226613
geneviewrs11226613
scholarrs11226613
googlers11226613
pharmgkbrs11226613
gwascentralrs11226613
openSNPrs11226613
23andMers11226613
23andMe allrs11226613
SNP Nexus

SNPshotrs11226613
SNPdbers11226613
MSV3drs11226613
GWAS Ctlgrs11226613
GMAF0.2052
Max Magnitude
? (A;A) (A;T) (T;T) 28
GWAS snp
PMID [PMID 23897914OA-icon.png]
Trait Bronchopulmonary dysplasia
Title A genome-wide association study (GWAS) for bronchopulmonary dysplasia.
Risk Allele T
P-val 5E-6
Odds Ratio 1.43 [0.6-0.81]