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rs587776734

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587776734(C;T)
Make rs587776734(T;T)
ReferenceGRCh38 38.1/142
ChromosomeX
Position155264073
GeneRAB39B
is asnp
is mentioned by
dbSNPrs587776734
ebirs587776734
HLIrs587776734
Exacrs587776734
Varsomers587776734
Maprs587776734
PheGenIrs587776734
hapmaprs587776734
1000 genomesrs587776734
hgdprs587776734
ensemblrs587776734
gopubmedrs587776734
geneviewrs587776734
scholarrs587776734
googlers587776734
pharmgkbrs587776734
gwascentralrs587776734
openSNPrs587776734
23andMers587776734
23andMe allrs587776734
SNP Nexus

SNPshotrs587776734
SNPdbers587776734
MSV3drs587776734
GWAS Ctlgrs587776734
Max Magnitude0
ClinVar
Risk rs587776734(C,T;C,T)
Alt rs587776734(C,T;C,T)
Reference rs587776734(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene RAB39B
CLNDBN Mental retardation, X-linked 72
Reversed 1
HGVS NC_000023.10:g.154493358C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011288.7,