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rs4302647

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs4302647(A;A)
Make rs4302647(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position94056539
is asnp
is mentioned by
dbSNPrs4302647
ebirs4302647
HLIrs4302647
Exacrs4302647
Varsomers4302647
Maprs4302647
PheGenIrs4302647
hapmaprs4302647
1000 genomesrs4302647
hgdprs4302647
ensemblrs4302647
gopubmedrs4302647
geneviewrs4302647
scholarrs4302647
googlers4302647
pharmgkbrs4302647
gwascentralrs4302647
openSNPrs4302647
23andMers4302647
23andMe allrs4302647
SNP Nexus

SNPshotrs4302647
SNPdbers4302647
MSV3drs4302647
GWAS Ctlgrs4302647
GMAF0.08494
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 21488853OA-icon.png] A genome-wide linkage screen in the Amish with Parkinson disease points to chromosome 6