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

rs730880272

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880272(G;T)
Make rs730880272(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position32493282
GeneFBXO7
is asnp
is mentioned by
dbSNPrs730880272
ebirs730880272
HLIrs730880272
Exacrs730880272
Varsomers730880272
Maprs730880272
PheGenIrs730880272
hapmaprs730880272
1000 genomesrs730880272
hgdprs730880272
ensemblrs730880272
gopubmedrs730880272
geneviewrs730880272
scholarrs730880272
googlers730880272
pharmgkbrs730880272
gwascentralrs730880272
openSNPrs730880272
23andMers730880272
23andMe allrs730880272
SNP Nexus

SNPshotrs730880272
SNPdbers730880272
MSV3drs730880272
GWAS Ctlgrs730880272
Max Magnitude0
ClinVar
Risk rs730880272(T;T)
Alt rs730880272(T;T)
Reference rs730880272(G;G)
Significance Pathogenic
Disease Parkinson disease 15
Variation info
Gene FBXO7
CLNDBN Parkinson disease 15
Reversed 0
HGVS NC_000022.10:g.32889269G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005079.3,