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rs17033506

From SNPedia

Orientationplus
Stabilizedplus
Make rs17033506(G;G)
Make rs17033506(G;T)
Make rs17033506(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position35598334
is asnp
is mentioned by
dbSNPrs17033506
ebirs17033506
HLIrs17033506
Exacrs17033506
Varsomers17033506
Maprs17033506
PheGenIrs17033506
hapmaprs17033506
1000 genomesrs17033506
hgdprs17033506
ensemblrs17033506
gopubmedrs17033506
geneviewrs17033506
scholarrs17033506
googlers17033506
pharmgkbrs17033506
gwascentralrs17033506
openSNPrs17033506
23andMers17033506
23andMe allrs17033506
SNP Nexus

SNPshotrs17033506
SNPdbers17033506
MSV3drs17033506
GWAS Ctlgrs17033506
GMAF0.03581
Max Magnitude
? (G;G) (G;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 4E-7
Odds Ratio NR NR