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rs3880457

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs3880457(C;C)
Make rs3880457(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31952442
GeneCFB, NELFE
is asnp
is mentioned by
dbSNPrs3880457
dbSNP (classic)rs3880457
ClinGenrs3880457
ebirs3880457
HLIrs3880457
Exacrs3880457
Gnomadrs3880457
Varsomers3880457
LitVarrs3880457
Maprs3880457
PheGenIrs3880457
Biobankrs3880457
1000 genomesrs3880457
hgdprs3880457
ensemblrs3880457
geneviewrs3880457
scholarrs3880457
googlers3880457
pharmgkbrs3880457
gwascentralrs3880457
openSNPrs3880457
23andMers3880457
SNPshotrs3880457
SNPdbers3880457
MSV3drs3880457
GWAS Ctlgrs3880457
GMAF0.0101
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 19556007] Role of RDBP and SKIV2L variants in the major histocompatibility complex class III region in polypoidal choroidal vasculopathy etiology