rs776576
From SNPedia
Merged into | rs541686 |
Orientation | plus |
Stabilized | plus |
Make rs776576(A;A) |
Make rs776576(A;G) |
Make rs776576(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 18745136 |
Gene | ADAMTSL1 |
is a | snp |
is | mentioned by |
dbSNP | rs776576 |
dbSNP (classic) | rs776576 |
ClinGen | rs776576 |
ebi | rs776576 |
HLI | rs776576 |
Exac | rs776576 |
Gnomad | rs776576 |
Varsome | rs776576 |
LitVar | rs776576 |
Map | rs776576 |
PheGenI | rs776576 |
Biobank | rs776576 |
1000 genomes | rs776576 |
hgdp | rs776576 |
ensembl | rs776576 |
geneview | rs776576 |
scholar | rs776576 |
rs776576 | |
pharmgkb | rs776576 |
gwascentral | rs776576 |
openSNP | rs776576 |
23andMe | rs776576 |
SNPshot | rs776576 |
SNPdbe | rs776576 |
MSV3d | rs776576 |
GWAS Ctlg | rs776576 |
Status | Merged into rs541686 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 21292647] 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