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rs431905511

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs431905511(A;A)
Make rs431905511(A;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position89828154
GeneSNCA
is asnp
is mentioned by
dbSNPrs431905511
ebirs431905511
HLIrs431905511
Exacrs431905511
Varsomers431905511
Maprs431905511
PheGenIrs431905511
hapmaprs431905511
1000 genomesrs431905511
hgdprs431905511
ensemblrs431905511
gopubmedrs431905511
geneviewrs431905511
scholarrs431905511
googlers431905511
pharmgkbrs431905511
gwascentralrs431905511
openSNPrs431905511
23andMers431905511
23andMe allrs431905511
SNP Nexus

SNPshotrs431905511
SNPdbers431905511
MSV3drs431905511
GWAS Ctlgrs431905511
Max Magnitude0
ClinVar
Risk rs431905511(A;A)
Alt rs431905511(A;A)
Reference rs431905511(G;G)
Significance Pathogenic
Disease Parkinson disease 1
Variation info
Gene SNCA
CLNDBN Parkinson disease 1
Reversed 1
HGVS NC_000004.11:g.90749305C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000083251.3,