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rs7698250

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common genotype
Make rs7698250(C;T)
Make rs7698250(T;T)
ReferenceGRCh38 38.1/142
Chromosome4
Position24514008
is asnp
is mentioned by
dbSNPrs7698250
dbSNP (classic)rs7698250
ClinGenrs7698250
ebirs7698250
HLIrs7698250
Exacrs7698250
Gnomadrs7698250
Varsomers7698250
LitVarrs7698250
Maprs7698250
PheGenIrs7698250
Biobankrs7698250
1000 genomesrs7698250
hgdprs7698250
ensemblrs7698250
geneviewrs7698250
scholarrs7698250
googlers7698250
pharmgkbrs7698250
gwascentralrs7698250
openSNPrs7698250
23andMers7698250
SNPshotrs7698250
SNPdbers7698250
MSV3drs7698250
GWAS Ctlgrs7698250
Max Magnitude0
? (C;C) (C;T) (T;T) 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 T
P-val 2E-10
Odds Ratio .46 [0.32-0.61] unit increase