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rs17077331

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs17077331(C;T)
Make rs17077331(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position65782209
is asnp
is mentioned by
dbSNPrs17077331
ebirs17077331
HLIrs17077331
Exacrs17077331
Varsomers17077331
Maprs17077331
PheGenIrs17077331
hapmaprs17077331
1000 genomesrs17077331
hgdprs17077331
ensemblrs17077331
gopubmedrs17077331
geneviewrs17077331
scholarrs17077331
googlers17077331
pharmgkbrs17077331
gwascentralrs17077331
openSNPrs17077331
23andMers17077331
23andMe allrs17077331
SNP Nexus

SNPshotrs17077331
SNPdbers17077331
MSV3drs17077331
GWAS Ctlgrs17077331
GMAF0.09504
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 0.000004
Odds Ratio 0.5048 None