rs497309
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common on affy axiom data |
Make rs497309(G;G) |
Make rs497309(G;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31924707 |
Gene | C2 |
is a | snp |
is | mentioned by |
dbSNP | rs497309 |
dbSNP (classic) | rs497309 |
ClinGen | rs497309 |
ebi | rs497309 |
HLI | rs497309 |
Exac | rs497309 |
Gnomad | rs497309 |
Varsome | rs497309 |
LitVar | rs497309 |
Map | rs497309 |
PheGenI | rs497309 |
Biobank | rs497309 |
1000 genomes | rs497309 |
hgdp | rs497309 |
ensembl | rs497309 |
geneview | rs497309 |
scholar | rs497309 |
rs497309 | |
pharmgkb | rs497309 |
gwascentral | rs497309 |
openSNP | rs497309 |
23andMe | rs497309 |
SNPshot | rs497309 |
SNPdbe | rs497309 |
MSV3d | rs497309 |
GWAS Ctlg | rs497309 |
GMAF | 0.0404 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 22170086] Polymorphisms in complement system genes and risk of non-Hodgkin lymphoma