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rs11905552

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs11905552(G;T)
Make rs11905552(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position3857753
GeneMAVS
is asnp
is mentioned by
dbSNPrs11905552
ebirs11905552
HLIrs11905552
Exacrs11905552
Varsomers11905552
Maprs11905552
PheGenIrs11905552
hapmaprs11905552
1000 genomesrs11905552
hgdprs11905552
ensemblrs11905552
gopubmedrs11905552
geneviewrs11905552
scholarrs11905552
googlers11905552
pharmgkbrs11905552
gwascentralrs11905552
openSNPrs11905552
23andMers11905552
23andMe allrs11905552
SNP Nexus

SNPshotrs11905552
SNPdbers11905552
MSV3drs11905552
GWAS Ctlgrs11905552
GMAF0.01745
Max Magnitude0
? (G;G) (G;T) (T;T) 28
[PMID 21268286OA-icon.png] A loss-of-function variant of the antiviral molecule MAVS is associated with a subset of systemic lupus patients