rs10836235
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10836235(C;C) |
Make rs10836235(C;T) |
Make rs10836235(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 34439157 |
Gene | CAT |
is a | snp |
is | mentioned by |
dbSNP | rs10836235 |
dbSNP (classic) | rs10836235 |
ClinGen | rs10836235 |
ebi | rs10836235 |
HLI | rs10836235 |
Exac | rs10836235 |
Gnomad | rs10836235 |
Varsome | rs10836235 |
LitVar | rs10836235 |
Map | rs10836235 |
PheGenI | rs10836235 |
Biobank | rs10836235 |
1000 genomes | rs10836235 |
hgdp | rs10836235 |
ensembl | rs10836235 |
geneview | rs10836235 |
scholar | rs10836235 |
rs10836235 | |
pharmgkb | rs10836235 |
gwascentral | rs10836235 |
openSNP | rs10836235 |
23andMe | rs10836235 |
SNPshot | rs10836235 |
SNPdbe | rs10836235 |
MSV3d | rs10836235 |
GWAS Ctlg | rs10836235 |
GMAF | 0.1534 |
Max Magnitude | 0 |
[PMID 19863340] Influence of the polymorphism in candidate genes on late cardiac damage in patients treated due to acute leukemia in childhood
[PMID 20416077] Identification of type 2 diabetes-associated combination of SNPs using support vector machine.