rs183805948
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs183805948(C;C) |
Make rs183805948(C;T) |
Make rs183805948(T;T) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 19 |
Position | 6720961 |
Gene | C3 |
is a | snp |
is | mentioned by |
dbSNP | rs183805948 |
dbSNP (classic) | rs183805948 |
ClinGen | rs183805948 |
ebi | rs183805948 |
HLI | rs183805948 |
Exac | rs183805948 |
Gnomad | rs183805948 |
Varsome | rs183805948 |
LitVar | rs183805948 |
Map | rs183805948 |
PheGenI | rs183805948 |
Biobank | rs183805948 |
1000 genomes | rs183805948 |
hgdp | rs183805948 |
ensembl | rs183805948 |
geneview | rs183805948 |
scholar | rs183805948 |
rs183805948 | |
pharmgkb | rs183805948 |
gwascentral | rs183805948 |
openSNP | rs183805948 |
23andMe | rs183805948 |
SNPshot | rs183805948 |
SNPdbe | rs183805948 |
MSV3d | rs183805948 |
GWAS Ctlg | rs183805948 |
Max Magnitude | 0 |
[PMID 28611769] Analysis of Complement C3 Gene Reveals Susceptibility to Severe Preeclampsia.