rs2241391
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2241391(A;A) |
Make rs2241391(A;G) |
Make rs2241391(G;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 19 |
Position | 6686493 |
Gene | C3 |
is a | snp |
is | mentioned by |
dbSNP | rs2241391 |
dbSNP (classic) | rs2241391 |
ClinGen | rs2241391 |
ebi | rs2241391 |
HLI | rs2241391 |
Exac | rs2241391 |
Gnomad | rs2241391 |
Varsome | rs2241391 |
LitVar | rs2241391 |
Map | rs2241391 |
PheGenI | rs2241391 |
Biobank | rs2241391 |
1000 genomes | rs2241391 |
hgdp | rs2241391 |
ensembl | rs2241391 |
geneview | rs2241391 |
scholar | rs2241391 |
rs2241391 | |
pharmgkb | rs2241391 |
gwascentral | rs2241391 |
openSNP | rs2241391 |
23andMe | rs2241391 |
SNPshot | rs2241391 |
SNPdbe | rs2241391 |
MSV3d | rs2241391 |
GWAS Ctlg | rs2241391 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 28611769] Analysis of Complement C3 Gene Reveals Susceptibility to Severe Preeclampsia.