rs61599409
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs61599409(C;C) |
Make rs61599409(C;T) |
Make rs61599409(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 8 |
Position | 96493302 |
Gene | SDC2 |
is a | snp |
is | mentioned by |
dbSNP | rs61599409 |
dbSNP (classic) | rs61599409 |
ClinGen | rs61599409 |
ebi | rs61599409 |
HLI | rs61599409 |
Exac | rs61599409 |
Gnomad | rs61599409 |
Varsome | rs61599409 |
LitVar | rs61599409 |
Map | rs61599409 |
PheGenI | rs61599409 |
Biobank | rs61599409 |
1000 genomes | rs61599409 |
hgdp | rs61599409 |
ensembl | rs61599409 |
geneview | rs61599409 |
scholar | rs61599409 |
rs61599409 | |
pharmgkb | rs61599409 |
gwascentral | rs61599409 |
openSNP | rs61599409 |
23andMe | rs61599409 |
SNPshot | rs61599409 |
SNPdbe | rs61599409 |
MSV3d | rs61599409 |
GWAS Ctlg | rs61599409 |
Max Magnitude | 0 |
[PMID 26463144] [Genetic variation in SDC2 is associated with the risk of radiation esophagitis in patients with esophageal squamous cell carcinoma receiving radiotherapy]