rs10494885
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs10494885(C;C) |
Make rs10494885(C;T) |
Make rs10494885(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 1 |
Position | 207641844 |
Gene | CR1 |
is a | snp |
is | mentioned by |
dbSNP | rs10494885 |
dbSNP (classic) | rs10494885 |
ClinGen | rs10494885 |
ebi | rs10494885 |
HLI | rs10494885 |
Exac | rs10494885 |
Gnomad | rs10494885 |
Varsome | rs10494885 |
LitVar | rs10494885 |
Map | rs10494885 |
PheGenI | rs10494885 |
Biobank | rs10494885 |
1000 genomes | rs10494885 |
hgdp | rs10494885 |
ensembl | rs10494885 |
geneview | rs10494885 |
scholar | rs10494885 |
rs10494885 | |
pharmgkb | rs10494885 |
gwascentral | rs10494885 |
openSNP | rs10494885 |
23andMe | rs10494885 |
SNPshot | rs10494885 |
SNPdbe | rs10494885 |
MSV3d | rs10494885 |
GWAS Ctlg | rs10494885 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 26000043] Complement receptor 1 genetic variants contribute to the susceptibility to gastric cancer in chinese population