rs9891263
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9891263(C;C) |
Make rs9891263(C;T) |
Make rs9891263(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 54859747 |
is a | snp |
is | mentioned by |
dbSNP | rs9891263 |
dbSNP (classic) | rs9891263 |
ClinGen | rs9891263 |
ebi | rs9891263 |
HLI | rs9891263 |
Exac | rs9891263 |
Gnomad | rs9891263 |
Varsome | rs9891263 |
LitVar | rs9891263 |
Map | rs9891263 |
PheGenI | rs9891263 |
Biobank | rs9891263 |
1000 genomes | rs9891263 |
hgdp | rs9891263 |
ensembl | rs9891263 |
geneview | rs9891263 |
scholar | rs9891263 |
rs9891263 | |
pharmgkb | rs9891263 |
gwascentral | rs9891263 |
openSNP | rs9891263 |
23andMe | rs9891263 |
SNPshot | rs9891263 |
SNPdbe | rs9891263 |
MSV3d | rs9891263 |
GWAS Ctlg | rs9891263 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 25227856] Exploratory investigation of genetic associations with Basal cell carcinoma risk: genome-wide association study in jeju island, Korea