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rs10799319

From SNPedia

Orientationplus
Stabilizedplus
Make rs10799319(A;A)
Make rs10799319(A;G)
Make rs10799319(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position225515783
GeneENAH
is asnp
is mentioned by
dbSNPrs10799319
ebirs10799319
HLIrs10799319
Exacrs10799319
Varsomers10799319
Maprs10799319
PheGenIrs10799319
hapmaprs10799319
1000 genomesrs10799319
hgdprs10799319
ensemblrs10799319
gopubmedrs10799319
geneviewrs10799319
scholarrs10799319
googlers10799319
pharmgkbrs10799319
gwascentralrs10799319
openSNPrs10799319
23andMers10799319
23andMe allrs10799319
SNP Nexus

SNPshotrs10799319
SNPdbers10799319
MSV3drs10799319
GWAS Ctlgrs10799319
GMAF0.3324
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 19641378OA-icon.png] The enabled homolog gene polymorphisms are associated with susceptibility and progression of childhood IgA nephropathy