rs163913
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs163913(C;C) |
Make rs163913(C;T) |
Make rs163913(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 6722624 |
Gene | C3 |
is a | snp |
is | mentioned by |
dbSNP | rs163913 |
dbSNP (classic) | rs163913 |
ClinGen | rs163913 |
ebi | rs163913 |
HLI | rs163913 |
Exac | rs163913 |
Gnomad | rs163913 |
Varsome | rs163913 |
LitVar | rs163913 |
Map | rs163913 |
PheGenI | rs163913 |
Biobank | rs163913 |
1000 genomes | rs163913 |
hgdp | rs163913 |
ensembl | rs163913 |
geneview | rs163913 |
scholar | rs163913 |
rs163913 | |
pharmgkb | rs163913 |
gwascentral | rs163913 |
openSNP | rs163913 |
23andMe | rs163913 |
SNPshot | rs163913 |
SNPdbe | rs163913 |
MSV3d | rs163913 |
GWAS Ctlg | rs163913 |
GMAF | 0.2328 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 19899988] Association of c3 gene polymorphisms with neovascular age-related macular degeneration in a chinese population
[PMID 19828715] Complement component 3 polymorphisms interact with polyunsaturated fatty acids to modulate risk of metabolic syndrome.