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

rs199624796

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199624796(A;A)
Make rs199624796(A;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position17004399
GeneATP13A2
is asnp
is mentioned by
dbSNPrs199624796
ebirs199624796
HLIrs199624796
Exacrs199624796
Varsomers199624796
Maprs199624796
PheGenIrs199624796
hapmaprs199624796
1000 genomesrs199624796
hgdprs199624796
ensemblrs199624796
gopubmedrs199624796
geneviewrs199624796
scholarrs199624796
googlers199624796
pharmgkbrs199624796
gwascentralrs199624796
openSNPrs199624796
23andMers199624796
23andMe allrs199624796
SNP Nexus

SNPshotrs199624796
SNPdbers199624796
MSV3drs199624796
GWAS Ctlgrs199624796
Max Magnitude0
ClinVar
Risk rs199624796(A;A)
Alt rs199624796(A;A)
Reference rs199624796(G;G)
Significance Pathogenic
Disease Parkinson disease 9
Variation info
Gene ATP13A2
CLNDBN Parkinson disease 9
Reversed 0
HGVS NC_000001.10:g.17330894G>A
CLNSRC ClinVar
CLNACC RCV000132730.1,