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rs776577

From SNPedia

Merged intors348334
Orientationplus
Stabilizedplus
Make rs776577(A;A)
Make rs776577(A;G)
Make rs776577(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position229587269
is asnp
is mentioned by
dbSNPrs776577
ebirs776577
HLIrs776577
Exacrs776577
Varsomers776577
Maprs776577
PheGenIrs776577
hapmaprs776577
1000 genomesrs776577
hgdprs776577
ensemblrs776577
gopubmedrs776577
geneviewrs776577
scholarrs776577
googlers776577
pharmgkbrs776577
gwascentralrs776577
openSNPrs776577
23andMers776577
23andMe allrs776577
SNP Nexus

SNPshotrs776577
SNPdbers776577
MSV3drs776577
GWAS Ctlgrs776577
StatusMerged into rs348334
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 21292647OA-icon.png] Association of a novel functional promoter variant (rs2075533 C>T) in the apoptosis gene TNFSF8 with risk of lung cancer - a finding from Texas lung cancer genome-wide association study