rs10825264
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs10825264(G;G) |
Make rs10825264(G;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 54188194 |
Gene | PCDH15 |
is a | snp |
is | mentioned by |
dbSNP | rs10825264 |
dbSNP (classic) | rs10825264 |
ClinGen | rs10825264 |
ebi | rs10825264 |
HLI | rs10825264 |
Exac | rs10825264 |
Gnomad | rs10825264 |
Varsome | rs10825264 |
LitVar | rs10825264 |
Map | rs10825264 |
PheGenI | rs10825264 |
Biobank | rs10825264 |
1000 genomes | rs10825264 |
hgdp | rs10825264 |
ensembl | rs10825264 |
geneview | rs10825264 |
scholar | rs10825264 |
rs10825264 | |
pharmgkb | rs10825264 |
gwascentral | rs10825264 |
openSNP | rs10825264 |
23andMe | rs10825264 |
SNPshot | rs10825264 |
SNPdbe | rs10825264 |
MSV3d | rs10825264 |
GWAS Ctlg | rs10825264 |
GMAF | 0.365 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 17701890] Identification of genetic variants contributing to cisplatin-induced cytotoxicity by use of a genomewide approach.