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rs4920608

From SNPedia

Orientationplus
Stabilizedplus
Make rs4920608(C;C)
Make rs4920608(C;T)
Make rs4920608(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position16992792
GeneATP13A2
is asnp
is mentioned by
dbSNPrs4920608
ebirs4920608
HLIrs4920608
Exacrs4920608
Varsomers4920608
Maprs4920608
PheGenIrs4920608
hapmaprs4920608
1000 genomesrs4920608
hgdprs4920608
ensemblrs4920608
gopubmedrs4920608
geneviewrs4920608
scholarrs4920608
googlers4920608
pharmgkbrs4920608
gwascentralrs4920608
openSNPrs4920608
23andMers4920608
23andMe allrs4920608
SNP Nexus

SNPshotrs4920608
SNPdbers4920608
MSV3drs4920608
GWAS Ctlgrs4920608
GMAF0.4573
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 22285144OA-icon.png] ATP13A2 (PARK9) polymorphisms influence the neurotoxic effects of manganese