rs3745567
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3745567(A;A) |
Make rs3745567(A;G) |
Make rs3745567(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 6690760 |
Gene | C3 |
is a | snp |
is | mentioned by |
dbSNP | rs3745567 |
dbSNP (classic) | rs3745567 |
ClinGen | rs3745567 |
ebi | rs3745567 |
HLI | rs3745567 |
Exac | rs3745567 |
Gnomad | rs3745567 |
Varsome | rs3745567 |
LitVar | rs3745567 |
Map | rs3745567 |
PheGenI | rs3745567 |
Biobank | rs3745567 |
1000 genomes | rs3745567 |
hgdp | rs3745567 |
ensembl | rs3745567 |
geneview | rs3745567 |
scholar | rs3745567 |
rs3745567 | |
pharmgkb | rs3745567 |
gwascentral | rs3745567 |
openSNP | rs3745567 |
23andMe | rs3745567 |
SNPshot | rs3745567 |
SNPdbe | rs3745567 |
MSV3d | rs3745567 |
GWAS Ctlg | rs3745567 |
GMAF | 0.0932 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23028341] |
Trait | Complement C3 and C4 levels |
Title | Genome-wide association study for serum complement C3 and C4 levels in healthy Chinese subjects. |
Risk Allele | T |
P-val | 2E-9 |
Odds Ratio | .09 [0.070-0.110] g/L increase |