rs2241392
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2241392(C;C) |
Make rs2241392(C;G) |
Make rs2241392(G;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 19 |
Position | 6685972 |
Gene | C3 |
is a | snp |
is | mentioned by |
dbSNP | rs2241392 |
dbSNP (classic) | rs2241392 |
ClinGen | rs2241392 |
ebi | rs2241392 |
HLI | rs2241392 |
Exac | rs2241392 |
Gnomad | rs2241392 |
Varsome | rs2241392 |
LitVar | rs2241392 |
Map | rs2241392 |
PheGenI | rs2241392 |
Biobank | rs2241392 |
1000 genomes | rs2241392 |
hgdp | rs2241392 |
ensembl | rs2241392 |
geneview | rs2241392 |
scholar | rs2241392 |
rs2241392 | |
pharmgkb | rs2241392 |
gwascentral | rs2241392 |
openSNP | rs2241392 |
23andMe | rs2241392 |
SNPshot | rs2241392 |
SNPdbe | rs2241392 |
MSV3d | rs2241392 |
GWAS Ctlg | rs2241392 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 29742493] Association Between Polymorphisms of the Complement 3 Gene and Schizophrenia in a Han Chinese Population.