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rs17218161

From SNPedia

Orientationplus
Stabilizedplus
Make rs17218161(C;C)
Make rs17218161(C;T)
Make rs17218161(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position58347679
is asnp
is mentioned by
dbSNPrs17218161
ebirs17218161
HLIrs17218161
Exacrs17218161
Varsomers17218161
Maprs17218161
PheGenIrs17218161
hapmaprs17218161
1000 genomesrs17218161
hgdprs17218161
ensemblrs17218161
gopubmedrs17218161
geneviewrs17218161
scholarrs17218161
googlers17218161
pharmgkbrs17218161
gwascentralrs17218161
openSNPrs17218161
23andMers17218161
23andMe allrs17218161
SNP Nexus

SNPshotrs17218161
SNPdbers17218161
MSV3drs17218161
GWAS Ctlgrs17218161
GMAF0.01837
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 2E-8
Odds Ratio NR NR