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rs398122405

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398122405(C;T)
Make rs398122405(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position65406052
GeneDNAJC6
is asnp
is mentioned by
dbSNPrs398122405
ebirs398122405
HLIrs398122405
Exacrs398122405
Varsomers398122405
Maprs398122405
PheGenIrs398122405
hapmaprs398122405
1000 genomesrs398122405
hgdprs398122405
ensemblrs398122405
gopubmedrs398122405
geneviewrs398122405
scholarrs398122405
googlers398122405
pharmgkbrs398122405
gwascentralrs398122405
openSNPrs398122405
23andMers398122405
23andMe allrs398122405
SNP Nexus

SNPshotrs398122405
SNPdbers398122405
MSV3drs398122405
GWAS Ctlgrs398122405
Max Magnitude0
ClinVar
Risk rs398122405(T;T)
Alt rs398122405(T;T)
Reference rs398122405(C;C)
Significance Pathogenic
Disease Parkinson disease 19a
Variation info
Gene DNAJC6
CLNDBN Parkinson disease 19a, juvenile-onset
Reversed 0
HGVS NC_000001.10:g.65871735C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000074443.4,