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rs9904270

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs9904270(C;T)
Make rs9904270(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position40323579
GeneLOC105371934, RARA
is asnp
is mentioned by
dbSNPrs9904270
dbSNP (classic)rs9904270
ClinGenrs9904270
ebirs9904270
HLIrs9904270
Exacrs9904270
Gnomadrs9904270
Varsomers9904270
LitVarrs9904270
Maprs9904270
PheGenIrs9904270
Biobankrs9904270
1000 genomesrs9904270
hgdprs9904270
ensemblrs9904270
geneviewrs9904270
scholarrs9904270
googlers9904270
pharmgkbrs9904270
gwascentralrs9904270
openSNPrs9904270
23andMers9904270
SNPshotrs9904270
SNPdbers9904270
MSV3drs9904270
GWAS Ctlgrs9904270
GMAF0.18
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 19233139] A novel polymorphism in CDC6 is associated with the decline in lung function of ex-smokers in COPD.


[PMID 18254975OA-icon.png] Physiogenomic comparison of human fat loss in response to diets restrictive of carbohydrate or fat.