rs2287845
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs2287845(C;T) |
Make rs2287845(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 19 |
Position | 6696586 |
Gene | C3 |
is a | snp |
is | mentioned by |
dbSNP | rs2287845 |
dbSNP (classic) | rs2287845 |
ClinGen | rs2287845 |
ebi | rs2287845 |
HLI | rs2287845 |
Exac | rs2287845 |
Gnomad | rs2287845 |
Varsome | rs2287845 |
LitVar | rs2287845 |
Map | rs2287845 |
PheGenI | rs2287845 |
Biobank | rs2287845 |
1000 genomes | rs2287845 |
hgdp | rs2287845 |
ensembl | rs2287845 |
geneview | rs2287845 |
scholar | rs2287845 |
rs2287845 | |
pharmgkb | rs2287845 |
gwascentral | rs2287845 |
openSNP | rs2287845 |
23andMe | rs2287845 |
SNPshot | rs2287845 |
SNPdbe | rs2287845 |
MSV3d | rs2287845 |
GWAS Ctlg | rs2287845 |
Max Magnitude | 0 |
[PMID 28611769] Analysis of Complement C3 Gene Reveals Susceptibility to Severe Preeclampsia.
ClinVar | |
---|---|
Risk | rs2287845(T;T) |
Alt | rs2287845(T;T) |
Reference | Rs2287845(C;C) |
Significance | Non-pathogenic |
Disease | C3 deficiency Macular degeneration Atypical hemolytic uremic syndrome |
Variation | info |
Gene | C3 |
CLNDBN | C3 deficiency Macular degeneration Atypical hemolytic uremic syndrome |
Reversed | 1 |
HGVS | NC_000019.9:g.6696597G>A |
CLNSRC | |
CLNACC | RCV000281934.1, RCV000317538.1, RCV000374021.1, |