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rs9883878

From SNPedia

Orientationplus
Stabilizedplus
Make rs9883878(A;A)
Make rs9883878(A;G)
Make rs9883878(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position178137844
is asnp
is mentioned by
dbSNPrs9883878
ebirs9883878
HLIrs9883878
Exacrs9883878
Varsomers9883878
Maprs9883878
PheGenIrs9883878
hapmaprs9883878
1000 genomesrs9883878
hgdprs9883878
ensemblrs9883878
gopubmedrs9883878
geneviewrs9883878
scholarrs9883878
googlers9883878
pharmgkbrs9883878
gwascentralrs9883878
openSNPrs9883878
23andMers9883878
23andMe allrs9883878
SNP Nexus

SNPshotrs9883878
SNPdbers9883878
MSV3drs9883878
GWAS Ctlgrs9883878
GMAF0.03076
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 1E-6
Odds Ratio NR NR