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rs2291667

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs2291667(C;T)
Make rs2291667(T;T)
ReferenceGRCh38 38.1/142
Chromosome19
Position6669975
GeneTNFSF14
is asnp
is mentioned by
dbSNPrs2291667
ebirs2291667
HLIrs2291667
Exacrs2291667
Varsomers2291667
Maprs2291667
PheGenIrs2291667
hapmaprs2291667
1000 genomesrs2291667
hgdprs2291667
ensemblrs2291667
gopubmedrs2291667
geneviewrs2291667
scholarrs2291667
googlers2291667
pharmgkbrs2291667
gwascentralrs2291667
openSNPrs2291667
23andMers2291667
23andMe allrs2291667
SNP Nexus

SNPshotrs2291667
SNPdbers2291667
MSV3drs2291667
GWAS Ctlgrs2291667
GMAF0.003673
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 20592286OA-icon.png] Polymorphic Variants of LIGHT (TNF Superfamily-14) Alter Receptor Avidity and Bioavailability