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rs4149579

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 1 Tumor Necrosis Factor 1A Receptor Intron Variant Homozygous
(G;G) 0 common in complete genomics
Make rs4149579(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position6338191
GeneTNFRSF1A
is asnp
is mentioned by
dbSNPrs4149579
ebirs4149579
HLIrs4149579
Exacrs4149579
Varsomers4149579
Maprs4149579
PheGenIrs4149579
hapmaprs4149579
1000 genomesrs4149579
hgdprs4149579
ensemblrs4149579
gopubmedrs4149579
geneviewrs4149579
scholarrs4149579
googlers4149579
pharmgkbrs4149579
gwascentralrs4149579
openSNPrs4149579
23andMers4149579
23andMe allrs4149579
SNP Nexus

SNPshotrs4149579
SNPdbers4149579
MSV3drs4149579
GWAS Ctlgrs4149579
GMAF0.03535
Max Magnitude1
? (A;A) (A;G) (G;G) 28

c.39+3585G>A is a rare SNV in an intronic region of TNFRSF1A, the gene for tumor necrosis factor receptor 1A.


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