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

rs387906832

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906832(A;A)
Make rs387906832(A;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position27509877
GeneRAB18
is asnp
is mentioned by
dbSNPrs387906832
ebirs387906832
HLIrs387906832
Exacrs387906832
Varsomers387906832
Maprs387906832
PheGenIrs387906832
hapmaprs387906832
1000 genomesrs387906832
hgdprs387906832
ensemblrs387906832
gopubmedrs387906832
geneviewrs387906832
scholarrs387906832
googlers387906832
pharmgkbrs387906832
gwascentralrs387906832
openSNPrs387906832
23andMers387906832
23andMe allrs387906832
SNP Nexus

SNPshotrs387906832
SNPdbers387906832
MSV3drs387906832
GWAS Ctlgrs387906832
Max Magnitude0
ClinVar
Risk rs387906832(A;A)
Alt rs387906832(A;A)
Reference rs387906832(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.27798806T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023171.5,