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rs17086172

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common genotype
Make rs17086172(C;C)
Make rs17086172(C;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position72559786
GeneCBLN2
is asnp
is mentioned by
dbSNPrs17086172
dbSNP (classic)rs17086172
ClinGenrs17086172
ebirs17086172
HLIrs17086172
Exacrs17086172
Gnomadrs17086172
Varsomers17086172
LitVarrs17086172
Maprs17086172
PheGenIrs17086172
Biobankrs17086172
1000 genomesrs17086172
hgdprs17086172
ensemblrs17086172
geneviewrs17086172
scholarrs17086172
googlers17086172
pharmgkbrs17086172
gwascentralrs17086172
openSNPrs17086172
23andMers17086172
SNPshotrs17086172
SNPdbers17086172
MSV3drs17086172
GWAS Ctlgrs17086172
GMAF0.073
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 22837378OA-icon.png]
Trait Airflow obstruction
Title Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.
Risk Allele
P-val 7E-6
Odds Ratio 1.35


[PMID 19300500OA-icon.png] A genome-wide association study of pulmonary function measures in the Framingham Heart Study.