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rs864309527

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864309527(A;A)
Make rs864309527(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position155260871
GeneRAB39B
is asnp
is mentioned by
dbSNPrs864309527
ebirs864309527
HLIrs864309527
Exacrs864309527
Varsomers864309527
Maprs864309527
PheGenIrs864309527
hapmaprs864309527
1000 genomesrs864309527
hgdprs864309527
ensemblrs864309527
gopubmedrs864309527
geneviewrs864309527
scholarrs864309527
googlers864309527
pharmgkbrs864309527
gwascentralrs864309527
openSNPrs864309527
23andMers864309527
23andMe allrs864309527
SNP Nexus

SNPshotrs864309527
SNPdbers864309527
MSV3drs864309527
GWAS Ctlgrs864309527
Max Magnitude0
ClinVar
Risk rs864309527(A;A)
Alt rs864309527(A;A)
Reference rs864309527(G;G)
Significance Pathogenic
Disease X-linked dominant Parkinson's disease Parkinsonism
Variation info
Gene RAB39B
CLNDBN X-linked dominant Parkinson's disease Parkinsonism, early onset with mental retardation
Reversed 1
HGVS NC_000023.10:g.154490156C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000202604.1, RCV000207511.1,