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rs121917767

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121917767(C;G)
Make rs121917767(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position41260751
GeneUCHL1
is asnp
is mentioned by
dbSNPrs121917767
ebirs121917767
HLIrs121917767
Exacrs121917767
Varsomers121917767
Maprs121917767
PheGenIrs121917767
hapmaprs121917767
1000 genomesrs121917767
hgdprs121917767
ensemblrs121917767
gopubmedrs121917767
geneviewrs121917767
scholarrs121917767
googlers121917767
pharmgkbrs121917767
gwascentralrs121917767
openSNPrs121917767
23andMers121917767
23andMe allrs121917767
SNP Nexus

SNPshotrs121917767
SNPdbers121917767
MSV3drs121917767
GWAS Ctlgrs121917767
Max Magnitude0
OMIM191342
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121917767(G,T;G,T)
Alt rs121917767(G,T;G,T)
Reference rs121917767(C;C)
Significance Other
Disease Parkinson disease 5
Variation info
Gene UCHL1
CLNDBN Parkinson disease 5
Reversed 0
HGVS NC_000004.11:g.41262768C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000013091.26,