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rs4926

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs4926(A;A)
Make rs4926(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position57614516
GeneSERPING1
is asnp
is mentioned by
dbSNPrs4926
dbSNP (classic)rs4926
ClinGenrs4926
ebirs4926
HLIrs4926
Exacrs4926
Gnomadrs4926
Varsomers4926
LitVarrs4926
Maprs4926
PheGenIrs4926
Biobankrs4926
1000 genomesrs4926
hgdprs4926
ensemblrs4926
geneviewrs4926
scholarrs4926
googlers4926
pharmgkbrs4926
gwascentralrs4926
openSNPrs4926
23andMers4926
SNPshotrs4926
SNPdbers4926
MSV3drs4926
GWAS Ctlgrs4926
GMAF0.1694
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 20062564OA-icon.png] An association study of SERPING1 gene and age-related macular degeneration in a Han Chinese population


[PMID 19169411OA-icon.png] Common variation in the SERPING1 gene is not associated with age-related macular degeneration in two independent groups of subjects.


[PMID 20161815OA-icon.png] SERPING1 polymorphisms in polypoidal choroidal vasculopathy.


[PMID 21385363OA-icon.png] Polymorphisms in genes controlling inflammation and tissue repair in rheumatoid arthritis: a case control study.


[PMID 21671989OA-icon.png] Dosing equation for tacrolimus using genetic variants and clinical factors.



ClinVar
Risk rs4926(A;A)
Alt rs4926(A;A)
Reference Rs4926(G;G)
Significance Non-pathogenic
Disease not specified Hereditary Angioedema
Variation info
Gene SERPING1
CLNDBN not specified Hereditary Angioedema
Reversed 0
HGVS NC_000011.9:g.57381989G>A
CLNSRC
CLNACC RCV000250736.1, RCV000288563.1,