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rs4416442

From SNPedia

Orientationplus
Stabilizedplus
Make rs4416442(C;C)
Make rs4416442(C;T)
Make rs4416442(T;T)
ReferenceGRCh38 38.1/142
Chromosome4
Position88945562
GeneFAM13A, LOC105377327
is asnp
is mentioned by
dbSNPrs4416442
dbSNP (classic)rs4416442
ClinGenrs4416442
ebirs4416442
HLIrs4416442
Exacrs4416442
Gnomadrs4416442
Varsomers4416442
LitVarrs4416442
Maprs4416442
PheGenIrs4416442
Biobankrs4416442
1000 genomesrs4416442
hgdprs4416442
ensemblrs4416442
geneviewrs4416442
scholarrs4416442
googlers4416442
pharmgkbrs4416442
gwascentralrs4416442
openSNPrs4416442
23andMers4416442
SNPshotrs4416442
SNPdbers4416442
MSV3drs4416442
GWAS Ctlgrs4416442
Max Magnitude0
GWAS snp
PMID [PMID 24621683OA-icon.png]
Trait Chronic obstructive pulmonary disease (moderate to severe)
Title Risk loci for chronic obstructive pulmonary disease: a genome-wide association study and meta-analysis.
Risk Allele C
P-val 1E-14
Odds Ratio 1.28 [1.20-1.36]