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rs886448

From SNPedia

Orientationminus
Stabilizedminus
Make rs886448(C;C)
Make rs886448(C;T)
Make rs886448(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position24200546
GeneLOC107986777
is asnp
is mentioned by
dbSNPrs886448
dbSNP (old)rs886448
ClinGenrs886448
ebirs886448
HLIrs886448
Exacrs886448
Gnomadrs886448
Varsomers886448
Maprs886448
PheGenIrs886448
Biobankrs886448
1000 genomesrs886448
hgdprs886448
ensemblrs886448
gopubmedrs886448
geneviewrs886448
scholarrs886448
googlers886448
pharmgkbrs886448
gwascentralrs886448
openSNPrs886448
23andMers886448
23andMe allrs886448
SNP Nexus

SNPshotrs886448
SNPdbers886448
MSV3drs886448
GWAS Ctlgrs886448
GMAF0.002296
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 7E-8
Odds Ratio NR NR