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rs587777874

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777874(A;A)
Make rs587777874(A;C)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position155260942
GeneRAB39B
is asnp
is mentioned by
dbSNPrs587777874
ebirs587777874
HLIrs587777874
Exacrs587777874
Varsomers587777874
Maprs587777874
PheGenIrs587777874
hapmaprs587777874
1000 genomesrs587777874
hgdprs587777874
ensemblrs587777874
gopubmedrs587777874
geneviewrs587777874
scholarrs587777874
googlers587777874
pharmgkbrs587777874
gwascentralrs587777874
openSNPrs587777874
23andMers587777874
23andMe allrs587777874
SNP Nexus

SNPshotrs587777874
SNPdbers587777874
MSV3drs587777874
GWAS Ctlgrs587777874
Max Magnitude0
ClinVar
Risk rs587777874(A;A)
Alt rs587777874(A;A)
Reference rs587777874(C;C)
Significance Pathogenic
Disease not provided Parkinsonism
Variation info
Gene RAB39B
CLNDBN not provided Parkinsonism, early onset with mental retardation
Reversed 1
HGVS NC_000023.10:g.154490227G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000144685.1, RCV000150034.3,