rs3738815

Orientation

minus

Stabilized

minus

Make rs3738815(A;A)

Make rs3738815(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

16988207

Gene

ATP13A2

is a	snp
is	mentioned by
dbSNP	rs3738815
dbSNP (classic)	rs3738815
ClinGen	rs3738815
ebi	rs3738815
HLI	rs3738815
Exac	rs3738815
Gnomad	rs3738815
Varsome	rs3738815
LitVar	rs3738815
Map	rs3738815
PheGenI	rs3738815
Biobank	rs3738815
1000 genomes	rs3738815
hgdp	rs3738815
ensembl	rs3738815
geneview	rs3738815
scholar	rs3738815
google	rs3738815
pharmgkb	rs3738815
gwascentral	rs3738815
openSNP	rs3738815
23andMe	rs3738815
SNPshot	rs3738815
SNPdbe	rs3738815
MSV3d	rs3738815
GWAS Ctlg	rs3738815

GMAF

0.3081

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

[PMID 22285144] ATP13A2 (PARK9) polymorphisms influence the neurotoxic effects of manganese

[PMID 19085912] ATP13A2 variability in Parkinson disease.

ClinVar
Risk	rs3738815(A;A) rs3738815(T;T)
Alt	rs3738815(A;A) rs3738815(T;T)
Reference	Rs3738815(G;G)
Significance	Non-pathogenic
Disease	not specified Parkinson disease 9
Variation	info
Gene	ATP13A2
CLNDBN	not specified Parkinson disease 9
Reversed	1
HGVS	NC_000001.10:g.17314702C>T
CLNSRC	ClinVar
CLNACC	RCV000116437.2, RCV000281364.1,