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rs121918305

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918305(C;T)
Make rs121918305(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position32475067
GeneFBXO7
is asnp
is mentioned by
dbSNPrs121918305
ebirs121918305
HLIrs121918305
Exacrs121918305
Varsomers121918305
Maprs121918305
PheGenIrs121918305
hapmaprs121918305
1000 genomesrs121918305
hgdprs121918305
ensemblrs121918305
gopubmedrs121918305
geneviewrs121918305
scholarrs121918305
googlers121918305
pharmgkbrs121918305
gwascentralrs121918305
openSNPrs121918305
23andMers121918305
23andMe allrs121918305
SNP Nexus

SNPshotrs121918305
SNPdbers121918305
MSV3drs121918305
GWAS Ctlgrs121918305
Max Magnitude0
OMIM605648
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121918305(T;T)
Alt rs121918305(T;T)
Reference rs121918305(C;C)
Significance Pathogenic
Disease Parkinson disease 15
Variation info
Gene FBXO7
CLNDBN Parkinson disease 15
Reversed 0
HGVS NC_000022.10:g.32871054C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005080.3,