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rs576861

From SNPedia

Orientationplus
Stabilizedplus
Make rs576861(C;C)
Make rs576861(C;T)
Make rs576861(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position225556635
GeneENAH
is asnp
is mentioned by
dbSNPrs576861
dbSNP (classic)rs576861
ClinGenrs576861
ebirs576861
HLIrs576861
Exacrs576861
Gnomadrs576861
Varsomers576861
LitVarrs576861
Maprs576861
PheGenIrs576861
Biobankrs576861
1000 genomesrs576861
hgdprs576861
ensemblrs576861
geneviewrs576861
scholarrs576861
googlers576861
pharmgkbrs576861
gwascentralrs576861
openSNPrs576861
23andMers576861
SNPshotrs576861
SNPdbers576861
MSV3drs576861
GWAS Ctlgrs576861
GMAF0.3333
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 19641378OA-icon.png] The enabled homolog gene polymorphisms are associated with susceptibility and progression of childhood IgA nephropathy