rs9418990
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9418990(C;C) |
Make rs9418990(C;T) |
Make rs9418990(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 133524462 |
Gene | LOC107984284 |
is a | snp |
is | mentioned by |
dbSNP | rs9418990 |
dbSNP (classic) | rs9418990 |
ClinGen | rs9418990 |
ebi | rs9418990 |
HLI | rs9418990 |
Exac | rs9418990 |
Gnomad | rs9418990 |
Varsome | rs9418990 |
LitVar | rs9418990 |
Map | rs9418990 |
PheGenI | rs9418990 |
Biobank | rs9418990 |
1000 genomes | rs9418990 |
hgdp | rs9418990 |
ensembl | rs9418990 |
geneview | rs9418990 |
scholar | rs9418990 |
rs9418990 | |
pharmgkb | rs9418990 |
gwascentral | rs9418990 |
openSNP | rs9418990 |
23andMe | rs9418990 |
SNPshot | rs9418990 |
SNPdbe | rs9418990 |
MSV3d | rs9418990 |
GWAS Ctlg | rs9418990 |
GMAF | 0.4362 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
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[PMID 19805575] A Case-Control and a Family-Based Association Study Revealing an Association between CYP2E1 Polymorphisms and Nasopharyngeal Carcinoma Risk in Cantonese