rs25681
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs25681(C;T) |
Make rs25681(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 121017727 |
Gene | C5 |
is a | snp |
is | mentioned by |
dbSNP | rs25681 |
dbSNP (classic) | rs25681 |
ClinGen | rs25681 |
ebi | rs25681 |
HLI | rs25681 |
Exac | rs25681 |
Gnomad | rs25681 |
Varsome | rs25681 |
LitVar | rs25681 |
Map | rs25681 |
PheGenI | rs25681 |
Biobank | rs25681 |
1000 genomes | rs25681 |
hgdp | rs25681 |
ensembl | rs25681 |
geneview | rs25681 |
scholar | rs25681 |
rs25681 | |
pharmgkb | rs25681 |
gwascentral | rs25681 |
openSNP | rs25681 |
23andMe | rs25681 |
SNPshot | rs25681 |
SNPdbe | rs25681 |
MSV3d | rs25681 |
GWAS Ctlg | rs25681 |
GMAF | 0.4082 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 19909405] Single nucleotide polymorphisms of complement component 5 and periodontitis
[PMID 21359210] Pooled genome-wide analysis to identify novel risk loci for pediatric allergic asthma.
[PMID 21393613] Association of complement 5 genetic polymorphism with renal allograft outcomes in Korea.
ClinVar | |
---|---|
Risk | rs25681(T;T) |
Alt | rs25681(T;T) |
Reference | Rs25681(C;C) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | C5 |
CLNDBN | not specified |
Reversed | 1 |
HGVS | NC_000009.11:g.123780005G>A |
CLNSRC | |
CLNACC | RCV000455480.1, |
[PMID 31570557] Association of TRAF1/C5 locus polymorphisms with epilepsy and clinical traits in Mexican neurocysticercosis patients.