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rs4704559

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs4704559(A;G)
Make rs4704559(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position79517086
is asnp
is mentioned by
dbSNPrs4704559
ebirs4704559
HLIrs4704559
Exacrs4704559
Varsomers4704559
Maprs4704559
PheGenIrs4704559
hapmaprs4704559
1000 genomesrs4704559
hgdprs4704559
ensemblrs4704559
gopubmedrs4704559
geneviewrs4704559
scholarrs4704559
googlers4704559
pharmgkbrs4704559
gwascentralrs4704559
openSNPrs4704559
23andMers4704559
23andMe allrs4704559
SNP Nexus

SNPshotrs4704559
SNPdbers4704559
MSV3drs4704559
GWAS Ctlgrs4704559
GMAF0.1469
Max Magnitude0
? (A;A) (A;G) (G;G) 28

[PMID 19648775] HOMER1 promoter analysis in Parkinson's disease: association study with psychotic symptoms