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rs7221059

From SNPedia

Orientationplus
Stabilizedplus
Make rs7221059(A;A)
Make rs7221059(A;C)
Make rs7221059(C;C)
ReferenceGRCh38 38.1/142
Chromosome17
Position76992362
is asnp
is mentioned by
dbSNPrs7221059
ebirs7221059
HLIrs7221059
Exacrs7221059
Varsomers7221059
Maprs7221059
PheGenIrs7221059
hapmaprs7221059
1000 genomesrs7221059
hgdprs7221059
ensemblrs7221059
gopubmedrs7221059
geneviewrs7221059
scholarrs7221059
googlers7221059
pharmgkbrs7221059
gwascentralrs7221059
openSNPrs7221059
23andMers7221059
23andMe allrs7221059
SNP Nexus

SNPshotrs7221059
SNPdbers7221059
MSV3drs7221059
GWAS Ctlgrs7221059
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 24383474OA-icon.png]
Trait Pulmonary emphysema
Title Genome-wide study of percent emphysema on computed tomography in the general population. The Multi-Ethnic Study of Atherosclerosis Lung/SNP Health Association Resource Study.
Risk Allele C
P-val 3E-8
Odds Ratio .33 [0.21-0.44] unit decrease