rs5746151
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common genotype |
Make rs5746151(A;A) |
Make rs5746151(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 6 |
Position | 159680288 |
Gene | SOD2 |
is a | snp |
is | mentioned by |
dbSNP | rs5746151 |
dbSNP (classic) | rs5746151 |
ClinGen | rs5746151 |
ebi | rs5746151 |
HLI | rs5746151 |
Exac | rs5746151 |
Gnomad | rs5746151 |
Varsome | rs5746151 |
LitVar | rs5746151 |
Map | rs5746151 |
PheGenI | rs5746151 |
Biobank | rs5746151 |
1000 genomes | rs5746151 |
hgdp | rs5746151 |
ensembl | rs5746151 |
geneview | rs5746151 |
scholar | rs5746151 |
rs5746151 | |
pharmgkb | rs5746151 |
gwascentral | rs5746151 |
openSNP | rs5746151 |
23andMe | rs5746151 |
SNPshot | rs5746151 |
SNPdbe | rs5746151 |
MSV3d | rs5746151 |
GWAS Ctlg | rs5746151 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 26400460] SOD2 genetic variant associated with treatment-related ototoxicity in cisplatin-treated pediatric medulloblastoma