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rs11141597

From SNPedia

Orientationplus
Stabilizedplus
Make rs11141597(A;A)
Make rs11141597(A;G)
Make rs11141597(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position86912543
is asnp
is mentioned by
dbSNPrs11141597
ebirs11141597
HLIrs11141597
Exacrs11141597
Varsomers11141597
Maprs11141597
PheGenIrs11141597
hapmaprs11141597
1000 genomesrs11141597
hgdprs11141597
ensemblrs11141597
gopubmedrs11141597
geneviewrs11141597
scholarrs11141597
googlers11141597
pharmgkbrs11141597
gwascentralrs11141597
openSNPrs11141597
23andMers11141597
23andMe allrs11141597
SNP Nexus

SNPshotrs11141597
SNPdbers11141597
MSV3drs11141597
GWAS Ctlgrs11141597
GMAF0.02204
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23829686OA-icon.png]
Trait Asthma (childhood onset)
Title Rank-based genome-wide analysis reveals the association of ryanodine receptor-2 gene variants with childhood asthma among human populations.
Risk Allele
P-val 2E-6
Odds Ratio NR NR