rs2287848
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2287848(C;C) |
Make rs2287848(C;T) |
Make rs2287848(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 19 |
Position | 6696331 |
Gene | C3 |
is a | snp |
is | mentioned by |
dbSNP | rs2287848 |
dbSNP (classic) | rs2287848 |
ClinGen | rs2287848 |
ebi | rs2287848 |
HLI | rs2287848 |
Exac | rs2287848 |
Gnomad | rs2287848 |
Varsome | rs2287848 |
LitVar | rs2287848 |
Map | rs2287848 |
PheGenI | rs2287848 |
Biobank | rs2287848 |
1000 genomes | rs2287848 |
hgdp | rs2287848 |
ensembl | rs2287848 |
geneview | rs2287848 |
scholar | rs2287848 |
rs2287848 | |
pharmgkb | rs2287848 |
gwascentral | rs2287848 |
openSNP | rs2287848 |
23andMe | rs2287848 |
SNPshot | rs2287848 |
SNPdbe | rs2287848 |
MSV3d | rs2287848 |
GWAS Ctlg | rs2287848 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 28611769] Analysis of Complement C3 Gene Reveals Susceptibility to Severe Preeclampsia.