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rs11098063

From SNPedia

Orientationplus
Stabilizedplus
Make rs11098063(C;C)
Make rs11098063(C;T)
Make rs11098063(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position110020646
is asnp
is mentioned by
dbSNPrs11098063
ebirs11098063
HLIrs11098063
Exacrs11098063
Varsomers11098063
Maprs11098063
PheGenIrs11098063
hapmaprs11098063
1000 genomesrs11098063
hgdprs11098063
ensemblrs11098063
gopubmedrs11098063
geneviewrs11098063
scholarrs11098063
googlers11098063
pharmgkbrs11098063
gwascentralrs11098063
openSNPrs11098063
23andMers11098063
23andMe allrs11098063
SNP Nexus

SNPshotrs11098063
SNPdbers11098063
MSV3drs11098063
GWAS Ctlgrs11098063
GMAF0.06336
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 23144319] Prognostic implications of genetic variants in advanced non-small cell lung cancer: a genome-wide association study