rs992670
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs992670(A;A) |
Make rs992670(A;G) |
Make rs992670(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 121019492 |
Gene | C5 |
is a | snp |
is | mentioned by |
dbSNP | rs992670 |
dbSNP (classic) | rs992670 |
ClinGen | rs992670 |
ebi | rs992670 |
HLI | rs992670 |
Exac | rs992670 |
Gnomad | rs992670 |
Varsome | rs992670 |
LitVar | rs992670 |
Map | rs992670 |
PheGenI | rs992670 |
Biobank | rs992670 |
1000 genomes | rs992670 |
hgdp | rs992670 |
ensembl | rs992670 |
geneview | rs992670 |
scholar | rs992670 |
rs992670 | |
pharmgkb | rs992670 |
gwascentral | rs992670 |
openSNP | rs992670 |
23andMe | rs992670 |
SNPshot | rs992670 |
SNPdbe | rs992670 |
MSV3d | rs992670 |
GWAS Ctlg | rs992670 |
GMAF | 0.4068 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19909405] Single nucleotide polymorphisms of complement component 5 and periodontitis
[PMID 31570557] Association of TRAF1/C5 locus polymorphisms with epilepsy and clinical traits in Mexican neurocysticercosis patients.