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rs387906833

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906833(C;C)
Make rs387906833(C;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position27538049
GeneRAB18
is asnp
is mentioned by
dbSNPrs387906833
ebirs387906833
HLIrs387906833
Exacrs387906833
Varsomers387906833
Maprs387906833
PheGenIrs387906833
hapmaprs387906833
1000 genomesrs387906833
hgdprs387906833
ensemblrs387906833
gopubmedrs387906833
geneviewrs387906833
scholarrs387906833
googlers387906833
pharmgkbrs387906833
gwascentralrs387906833
openSNPrs387906833
23andMers387906833
23andMe allrs387906833
SNP Nexus

SNPshotrs387906833
SNPdbers387906833
MSV3drs387906833
GWAS Ctlgrs387906833
Max Magnitude0
ClinVar
Risk rs387906833(C;C)
Alt rs387906833(C;C)
Reference rs387906833(T;T)
Significance Pathogenic
Disease Warburg micro syndrome 3
Variation info
Gene RAB18
CLNDBN Warburg micro syndrome 3
Reversed 0
HGVS NC_000010.10:g.27826978T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000023174.3,