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rs587777053

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587777053(A;C)
Make rs587777053(C;C)
ReferenceGRCh38 38.1/142
Chromosome1
Position16989739
GeneATP13A2
is asnp
is mentioned by
dbSNPrs587777053
ebirs587777053
HLIrs587777053
Exacrs587777053
Varsomers587777053
Maprs587777053
PheGenIrs587777053
hapmaprs587777053
1000 genomesrs587777053
hgdprs587777053
ensemblrs587777053
gopubmedrs587777053
geneviewrs587777053
scholarrs587777053
googlers587777053
pharmgkbrs587777053
gwascentralrs587777053
openSNPrs587777053
23andMers587777053
23andMe allrs587777053
SNP Nexus

SNPshotrs587777053
SNPdbers587777053
MSV3drs587777053
GWAS Ctlgrs587777053
Max Magnitude0
ClinVar
Risk rs587777053(A,C;A,C)
Alt rs587777053(A,C;A,C)
Reference rs587777053(T;T)
Significance Pathogenic
Disease Parkinson disease 9
Variation info
Gene ATP13A2
CLNDBN Parkinson disease 9
Reversed 1
HGVS NC_000001.10:g.17316234A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000056335.8,