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rs10187654

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs10187654(C;T)
Make rs10187654(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position233905414
is asnp
is mentioned by
dbSNPrs10187654
ebirs10187654
HLIrs10187654
Exacrs10187654
Varsomers10187654
Maprs10187654
PheGenIrs10187654
hapmaprs10187654
1000 genomesrs10187654
hgdprs10187654
ensemblrs10187654
gopubmedrs10187654
geneviewrs10187654
scholarrs10187654
googlers10187654
pharmgkbrs10187654
gwascentralrs10187654
openSNPrs10187654
23andMers10187654
23andMe allrs10187654
SNP Nexus

SNPshotrs10187654
SNPdbers10187654
MSV3drs10187654
GWAS Ctlgrs10187654
GMAF0.4692
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22424883OA-icon.png]
Trait
Title Genome-wide association study of lung function decline in adults with and without asthma.
Risk Allele
P-val 0.000009
Odds Ratio 0.1506 None