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rs2076600

From SNPedia

Orientationminus
Stabilizedminus
Make rs2076600(C;C)
Make rs2076600(C;T)
Make rs2076600(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position17010896
GeneATP13A2
is asnp
is mentioned by
dbSNPrs2076600
ebirs2076600
HLIrs2076600
Exacrs2076600
Varsomers2076600
Maprs2076600
PheGenIrs2076600
hapmaprs2076600
1000 genomesrs2076600
hgdprs2076600
ensemblrs2076600
gopubmedrs2076600
geneviewrs2076600
scholarrs2076600
googlers2076600
pharmgkbrs2076600
gwascentralrs2076600
openSNPrs2076600
23andMers2076600
23andMe allrs2076600
SNP Nexus

SNPshotrs2076600
SNPdbers2076600
MSV3drs2076600
GWAS Ctlgrs2076600
GMAF0.3875
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 22285144OA-icon.png] ATP13A2 (PARK9) polymorphisms influence the neurotoxic effects of manganese