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rs2473967

From SNPedia

Orientationminus
Stabilizedminus
Make rs2473967(A;A)
Make rs2473967(A;C)
Make rs2473967(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position113158133
is asnp
is mentioned by
dbSNPrs2473967
ebirs2473967
HLIrs2473967
Exacrs2473967
Varsomers2473967
Maprs2473967
PheGenIrs2473967
hapmaprs2473967
1000 genomesrs2473967
hgdprs2473967
ensemblrs2473967
gopubmedrs2473967
geneviewrs2473967
scholarrs2473967
googlers2473967
pharmgkbrs2473967
gwascentralrs2473967
openSNPrs2473967
23andMers2473967
23andMe allrs2473967
SNP Nexus

SNPshotrs2473967
SNPdbers2473967
MSV3drs2473967
GWAS Ctlgrs2473967
GMAF0.1162
Max Magnitude
? (A;A) (A;C) (C;C) 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-6
Odds Ratio NR NR