Have questions? Visit https://www.reddit.com/r/SNPedia

rs10189629

From SNPedia

Orientationplus
Stabilizedplus
Make rs10189629(A;A)
Make rs10189629(A;C)
Make rs10189629(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position102263004
is asnp
is mentioned by
dbSNPrs10189629
dbSNP (old)rs10189629
ClinGenrs10189629
ebirs10189629
HLIrs10189629
Exacrs10189629
Varsomers10189629
Maprs10189629
PheGenIrs10189629
Biobankrs10189629
1000 genomesrs10189629
hgdprs10189629
ensemblrs10189629
gopubmedrs10189629
geneviewrs10189629
scholarrs10189629
googlers10189629
pharmgkbrs10189629
gwascentralrs10189629
openSNPrs10189629
23andMers10189629
23andMe allrs10189629
SNP Nexus

SNPshotrs10189629
SNPdbers10189629
MSV3drs10189629
GWAS Ctlgrs10189629
GMAF0.1561
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23817569OA-icon.png]
Trait Self-reported allergy
Title A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci.
Risk Allele A
P-val 2E-16
Odds Ratio .14 [0.11-0.18] unit decrease