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rs2076602

From SNPedia

Orientationminus
Stabilizedminus
Make rs2076602(A;A)
Make rs2076602(A;T)
Make rs2076602(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position16996703
GeneATP13A2
is asnp
is mentioned by
dbSNPrs2076602
ebirs2076602
HLIrs2076602
Exacrs2076602
Varsomers2076602
Maprs2076602
PheGenIrs2076602
hapmaprs2076602
1000 genomesrs2076602
hgdprs2076602
ensemblrs2076602
gopubmedrs2076602
geneviewrs2076602
scholarrs2076602
googlers2076602
pharmgkbrs2076602
gwascentralrs2076602
openSNPrs2076602
23andMers2076602
23andMe allrs2076602
SNP Nexus

SNPshotrs2076602
SNPdbers2076602
MSV3drs2076602
GWAS Ctlgrs2076602
GMAF0.3085
Max Magnitude
? (A;A) (A;T) (T;T) 28
[PMID 22285144OA-icon.png] ATP13A2 (PARK9) polymorphisms influence the neurotoxic effects of manganese