rs17788084
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs17788084(A;A) |
Make rs17788084(A;T) |
Make rs17788084(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 8 |
Position | 96610720 |
Gene | SDC2 |
is a | snp |
is | mentioned by |
dbSNP | rs17788084 |
dbSNP (classic) | rs17788084 |
ClinGen | rs17788084 |
ebi | rs17788084 |
HLI | rs17788084 |
Exac | rs17788084 |
Gnomad | rs17788084 |
Varsome | rs17788084 |
LitVar | rs17788084 |
Map | rs17788084 |
PheGenI | rs17788084 |
Biobank | rs17788084 |
1000 genomes | rs17788084 |
hgdp | rs17788084 |
ensembl | rs17788084 |
geneview | rs17788084 |
scholar | rs17788084 |
rs17788084 | |
pharmgkb | rs17788084 |
gwascentral | rs17788084 |
openSNP | rs17788084 |
23andMe | rs17788084 |
SNPshot | rs17788084 |
SNPdbe | rs17788084 |
MSV3d | rs17788084 |
GWAS Ctlg | rs17788084 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
[PMID 26463144] [Genetic variation in SDC2 is associated with the risk of radiation esophagitis in patients with esophageal squamous cell carcinoma receiving radiotherapy]