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rs6054973

From SNPedia

Orientationplus
Stabilizedplus
Make rs6054973(C;C)
Make rs6054973(C;T)
Make rs6054973(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position7405311
is asnp
is mentioned by
dbSNPrs6054973
ebirs6054973
HLIrs6054973
Exacrs6054973
Varsomers6054973
Maprs6054973
PheGenIrs6054973
hapmaprs6054973
1000 genomesrs6054973
hgdprs6054973
ensemblrs6054973
gopubmedrs6054973
geneviewrs6054973
scholarrs6054973
googlers6054973
pharmgkbrs6054973
gwascentralrs6054973
openSNPrs6054973
23andMers6054973
23andMe allrs6054973
SNP Nexus

SNPshotrs6054973
SNPdbers6054973
MSV3drs6054973
GWAS Ctlgrs6054973
GMAF0.04591
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 1E-7
Odds Ratio NR NR