Have questions? Visit https://www.reddit.com/r/SNPedia

rs17483721

From SNPedia

Orientationplus
Stabilizedplus
Make rs17483721(C;C)
Make rs17483721(C;T)
Make rs17483721(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position78441389
GeneIREB2
is asnp
is mentioned by
dbSNPrs17483721
ebirs17483721
HLIrs17483721
Exacrs17483721
Varsomers17483721
Maprs17483721
PheGenIrs17483721
hapmaprs17483721
1000 genomesrs17483721
hgdprs17483721
ensemblrs17483721
gopubmedrs17483721
geneviewrs17483721
scholarrs17483721
googlers17483721
pharmgkbrs17483721
gwascentralrs17483721
openSNPrs17483721
23andMers17483721
23andMe allrs17483721
SNP Nexus

SNPshotrs17483721
SNPdbers17483721
MSV3drs17483721
GWAS Ctlgrs17483721
GMAF0.2649
Max Magnitude
? (C;C) (C;T) (T;T) 28
Rs17483721
PubMed [PMID 18385738]
Affy Probeset SNP_A-2286979
Affy Orientation same
On GW 5.0
Alleles A/B C/T
Ancestral T
Population Caucasian(Europe)
Allele C
Case Freq. 0.39
Control Freq. 0.34
Odds Ratio Het
Odds Ratio Hom
Odds Ratio All 1.27
Disease Lung cancer (LC)


rs17483721 increases susceptibility to Lung cancer 1.27 times for carriers of the C allele [PMID 18385738]


[PMID 18759969OA-icon.png] In search of causal variants: refining disease association signals using cross-population contrasts.