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rs25681

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs25681(C;T)
Make rs25681(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position121017727
GeneC5
is asnp
is mentioned by
dbSNPrs25681
dbSNP (classic)rs25681
ClinGenrs25681
ebirs25681
HLIrs25681
Exacrs25681
Gnomadrs25681
Varsomers25681
LitVarrs25681
Maprs25681
PheGenIrs25681
Biobankrs25681
1000 genomesrs25681
hgdprs25681
ensemblrs25681
geneviewrs25681
scholarrs25681
googlers25681
pharmgkbrs25681
gwascentralrs25681
openSNPrs25681
23andMers25681
SNPshotrs25681
SNPdbers25681
MSV3drs25681
GWAS Ctlgrs25681
GMAF0.4082
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 19909405] Single nucleotide polymorphisms of complement component 5 and periodontitis


[PMID 21359210OA-icon.png] 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 31570557OA-icon.png] Association of TRAF1/C5 locus polymorphisms with epilepsy and clinical traits in Mexican neurocysticercosis patients.