Have questions? Visit https://www.reddit.com/r/SNPedia

rs3738815

From SNPedia

Orientationminus
Stabilizedminus
Make rs3738815(A;A)
Make rs3738815(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position16988207
GeneATP13A2
is asnp
is mentioned by
dbSNPrs3738815
ebirs3738815
HLIrs3738815
Exacrs3738815
Varsomers3738815
Maprs3738815
PheGenIrs3738815
hapmaprs3738815
1000 genomesrs3738815
hgdprs3738815
ensemblrs3738815
gopubmedrs3738815
geneviewrs3738815
scholarrs3738815
googlers3738815
pharmgkbrs3738815
gwascentralrs3738815
openSNPrs3738815
23andMers3738815
23andMe allrs3738815
SNP Nexus

SNPshotrs3738815
SNPdbers3738815
MSV3drs3738815
GWAS Ctlgrs3738815
GMAF0.3081
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 22285144OA-icon.png] ATP13A2 (PARK9) polymorphisms influence the neurotoxic effects of manganese

[PMID 19085912OA-icon.png] ATP13A2 variability in Parkinson disease.


ClinVar
Risk rs3738815(A;A)
Alt rs3738815(A;A)
Reference rs3738815(G;G)
Significance Non-pathogenic
Disease not specified
Variation info
Gene ATP13A2
CLNDBN not specified
Reversed 1
HGVS NC_000001.10:g.17314702C>T
CLNSRC ClinVar
CLNACC RCV000116437.1,