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rs16929097

From SNPedia

Orientationplus
Stabilizedplus
Make rs16929097(A;A)
Make rs16929097(A;G)
Make rs16929097(G;G)
ReferenceGRCh37.p10 37.5/138
Chromosome9
Position12521826
is asnp
is mentioned by
dbSNPrs16929097
ebirs16929097
HLIrs16929097
Exacrs16929097
Varsomers16929097
Maprs16929097
PheGenIrs16929097
hapmaprs16929097
1000 genomesrs16929097
hgdprs16929097
ensemblrs16929097
gopubmedrs16929097
geneviewrs16929097
scholarrs16929097
googlers16929097
pharmgkbrs16929097
gwascentralrs16929097
openSNPrs16929097
23andMers16929097
23andMe allrs16929097
SNP Nexus

SNPshotrs16929097
SNPdbers16929097
MSV3drs16929097
GWAS Ctlgrs16929097
GMAF0.04178
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 8E-9
Odds Ratio NR NR