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rs6721181

From SNPedia

Orientationplus
Stabilizedplus
Make rs6721181(C;C)
Make rs6721181(C;T)
Make rs6721181(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position39888556
is asnp
is mentioned by
dbSNPrs6721181
ebirs6721181
HLIrs6721181
Exacrs6721181
Varsomers6721181
Maprs6721181
PheGenIrs6721181
hapmaprs6721181
1000 genomesrs6721181
hgdprs6721181
ensemblrs6721181
gopubmedrs6721181
geneviewrs6721181
scholarrs6721181
googlers6721181
pharmgkbrs6721181
gwascentralrs6721181
openSNPrs6721181
23andMers6721181
23andMe allrs6721181
SNP Nexus

SNPshotrs6721181
SNPdbers6721181
MSV3drs6721181
GWAS Ctlgrs6721181
GMAF0.01607
Max Magnitude
? (C;C) (C;T) (T;T) 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 6E-7
Odds Ratio NR NR