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rs12504628

From SNPedia

Orientationplus
Stabilizedplus
Make rs12504628(C;C)
Make rs12504628(C;T)
Make rs12504628(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position144515172
is asnp
is mentioned by
dbSNPrs12504628
ebirs12504628
HLIrs12504628
Exacrs12504628
Varsomers12504628
Maprs12504628
PheGenIrs12504628
hapmaprs12504628
1000 genomesrs12504628
hgdprs12504628
ensemblrs12504628
gopubmedrs12504628
geneviewrs12504628
scholarrs12504628
googlers12504628
pharmgkbrs12504628
gwascentralrs12504628
openSNPrs12504628
23andMers12504628
23andMe allrs12504628
SNP Nexus

SNPshotrs12504628
SNPdbers12504628
MSV3drs12504628
GWAS Ctlgrs12504628
GMAF0.3062
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20010834OA-icon.png]
Trait Lung function
Title Genome-wide association study identifies five loci associated with lung function
Risk Allele T
P-val 6E-13
Odds Ratio 0.27 [NR] % variance explained


[PMID 21965014OA-icon.png] Effect of five genetic variants associated with lung function on the risk of chronic obstructive lung disease, and their joint effects on lung function.


GET Evidence
rs12504628
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.257812
summary