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rs13147758

From SNPedia

Orientationplus
Stabilizedplus
Make rs13147758(A;A)
Make rs13147758(A;G)
Make rs13147758(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position144539078
is asnp
is mentioned by
dbSNPrs13147758
ebirs13147758
HLIrs13147758
Exacrs13147758
Varsomers13147758
Maprs13147758
PheGenIrs13147758
hapmaprs13147758
1000 genomesrs13147758
hgdprs13147758
ensemblrs13147758
gopubmedrs13147758
geneviewrs13147758
scholarrs13147758
googlers13147758
pharmgkbrs13147758
gwascentralrs13147758
openSNPrs13147758
23andMers13147758
23andMe allrs13147758
SNP Nexus

SNPshotrs13147758
SNPdbers13147758
MSV3drs13147758
GWAS Ctlgrs13147758
GMAF0.2952
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19300500OA-icon.png]
Trait Pulmonary function measures
Title A Genome-Wide Association Study of Pulmonary Function Measures in the Framingham Heart Study
Risk Allele G
P-val 8E-11
Odds Ratio 0.10 [NR] % increase in FEV1/FVC ratio



[PMID 20010834OA-icon.png] Genome-wide association study identifies five loci associated with lung function.


GET Evidence
rs13147758
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.257812
summary