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rs11785599

From SNPedia

Orientationplus
Stabilizedplus
Make rs11785599(C;C)
Make rs11785599(C;T)
Make rs11785599(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position23034761
GeneTNFRSF10B
is asnp
is mentioned by
dbSNPrs11785599
dbSNP (old)rs11785599
ClinGenrs11785599
ebirs11785599
HLIrs11785599
Exacrs11785599
Gnomadrs11785599
Varsomers11785599
Maprs11785599
PheGenIrs11785599
Biobankrs11785599
1000 genomesrs11785599
hgdprs11785599
ensemblrs11785599
gopubmedrs11785599
geneviewrs11785599
scholarrs11785599
googlers11785599
pharmgkbrs11785599
gwascentralrs11785599
openSNPrs11785599
23andMers11785599
23andMe allrs11785599
SNP Nexus

SNPshotrs11785599
SNPdbers11785599
MSV3drs11785599
GWAS Ctlgrs11785599
GMAF0.3825
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 23839018OA-icon.png] TNFRSF10B polymorphisms and haplotypes associated with increased risk of death in non-small cell lung cancer