rs10808555
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10808555(A;A) |
Make rs10808555(A;G) |
Make rs10808555(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 8 |
Position | 127397266 |
Gene | CASC8 |
is a | snp |
is | mentioned by |
dbSNP | rs10808555 |
dbSNP (classic) | rs10808555 |
ClinGen | rs10808555 |
ebi | rs10808555 |
HLI | rs10808555 |
Exac | rs10808555 |
Gnomad | rs10808555 |
Varsome | rs10808555 |
LitVar | rs10808555 |
Map | rs10808555 |
PheGenI | rs10808555 |
Biobank | rs10808555 |
1000 genomes | rs10808555 |
hgdp | rs10808555 |
ensembl | rs10808555 |
geneview | rs10808555 |
scholar | rs10808555 |
rs10808555 | |
pharmgkb | rs10808555 |
gwascentral | rs10808555 |
openSNP | rs10808555 |
23andMe | rs10808555 |
SNPshot | rs10808555 |
SNPdbe | rs10808555 |
MSV3d | rs10808555 |
GWAS Ctlg | rs10808555 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 27769063] Risk of eighteen genome-wide association study-identified genetic variants for colorectal cancer and colorectal adenoma in Han Chinese.