rs6089953
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6089953(A;A) |
Make rs6089953(A;G) |
Make rs6089953(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 20 |
Position | 63659655 |
Gene | RTEL1, RTEL1-TNFRSF6B |
is a | snp |
is | mentioned by |
dbSNP | rs6089953 |
dbSNP (classic) | rs6089953 |
ClinGen | rs6089953 |
ebi | rs6089953 |
HLI | rs6089953 |
Exac | rs6089953 |
Gnomad | rs6089953 |
Varsome | rs6089953 |
LitVar | rs6089953 |
Map | rs6089953 |
PheGenI | rs6089953 |
Biobank | rs6089953 |
1000 genomes | rs6089953 |
hgdp | rs6089953 |
ensembl | rs6089953 |
geneview | rs6089953 |
scholar | rs6089953 |
rs6089953 | |
pharmgkb | rs6089953 |
gwascentral | rs6089953 |
openSNP | rs6089953 |
23andMe | rs6089953 |
SNPshot | rs6089953 |
SNPdbe | rs6089953 |
MSV3d | rs6089953 |
GWAS Ctlg | rs6089953 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 26014354] CCDC26, CDKN2BAS, RTEL1 and TERT Polymorphisms in pediatric brain tumor susceptibility
[PMID 30462709] Association analysis of RTEL1 variants with risk of adult gliomas in a Korean population.