rs11672613
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11672613(C;C) |
Make rs11672613(C;T) |
Make rs11672613(T;T) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 19 |
Position | 6705235 |
Gene | C3 |
is a | snp |
is | mentioned by |
dbSNP | rs11672613 |
dbSNP (classic) | rs11672613 |
ClinGen | rs11672613 |
ebi | rs11672613 |
HLI | rs11672613 |
Exac | rs11672613 |
Gnomad | rs11672613 |
Varsome | rs11672613 |
LitVar | rs11672613 |
Map | rs11672613 |
PheGenI | rs11672613 |
Biobank | rs11672613 |
1000 genomes | rs11672613 |
hgdp | rs11672613 |
ensembl | rs11672613 |
geneview | rs11672613 |
scholar | rs11672613 |
rs11672613 | |
pharmgkb | rs11672613 |
gwascentral | rs11672613 |
openSNP | rs11672613 |
23andMe | rs11672613 |
SNPshot | rs11672613 |
SNPdbe | rs11672613 |
MSV3d | rs11672613 |
GWAS Ctlg | rs11672613 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 29742493] Association Between Polymorphisms of the Complement 3 Gene and Schizophrenia in a Han Chinese Population.