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rs150519745

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs150519745(C;T)
Make rs150519745(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position17000107
GeneATP13A2
is asnp
is mentioned by
dbSNPrs150519745
ebirs150519745
HLIrs150519745
Exacrs150519745
Varsomers150519745
Maprs150519745
PheGenIrs150519745
hapmaprs150519745
1000 genomesrs150519745
hgdprs150519745
ensemblrs150519745
gopubmedrs150519745
geneviewrs150519745
scholarrs150519745
googlers150519745
pharmgkbrs150519745
gwascentralrs150519745
openSNPrs150519745
23andMers150519745
23andMe allrs150519745
SNP Nexus

SNPshotrs150519745
SNPdbers150519745
MSV3drs150519745
GWAS Ctlgrs150519745
Max Magnitude0
ClinVar
Risk rs150519745(T;T)
Alt rs150519745(T;T)
Reference Rs150519745(C;C)
Significance Probable-Pathogenic
Disease Parkinson disease 9
Variation info
Gene ATP13A2
CLNDBN Parkinson disease 9
Reversed 0
HGVS NC_000001.10:g.17326602C>T
CLNSRC Baylor College of Medicine
CLNACC RCV000191065.1,