rs190390034
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs190390034(A;A) |
Make rs190390034(A;C) |
Make rs190390034(C;C) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 19 |
Position | 6719442 |
Gene | C3 |
is a | snp |
is | mentioned by |
dbSNP | rs190390034 |
dbSNP (classic) | rs190390034 |
ClinGen | rs190390034 |
ebi | rs190390034 |
HLI | rs190390034 |
Exac | rs190390034 |
Gnomad | rs190390034 |
Varsome | rs190390034 |
LitVar | rs190390034 |
Map | rs190390034 |
PheGenI | rs190390034 |
Biobank | rs190390034 |
1000 genomes | rs190390034 |
hgdp | rs190390034 |
ensembl | rs190390034 |
geneview | rs190390034 |
scholar | rs190390034 |
rs190390034 | |
pharmgkb | rs190390034 |
gwascentral | rs190390034 |
openSNP | rs190390034 |
23andMe | rs190390034 |
SNPshot | rs190390034 |
SNPdbe | rs190390034 |
MSV3d | rs190390034 |
GWAS Ctlg | rs190390034 |
Max Magnitude | 0 |
[PMID 28611769] Analysis of Complement C3 Gene Reveals Susceptibility to Severe Preeclampsia.