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rs587777151

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777151(C;G)
Make rs587777151(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position27533759
GeneRAB18
is asnp
is mentioned by
dbSNPrs587777151
ebirs587777151
HLIrs587777151
Exacrs587777151
Varsomers587777151
Maprs587777151
PheGenIrs587777151
hapmaprs587777151
1000 genomesrs587777151
hgdprs587777151
ensemblrs587777151
gopubmedrs587777151
geneviewrs587777151
scholarrs587777151
googlers587777151
pharmgkbrs587777151
gwascentralrs587777151
openSNPrs587777151
23andMers587777151
23andMe allrs587777151
SNP Nexus

SNPshotrs587777151
SNPdbers587777151
MSV3drs587777151
GWAS Ctlgrs587777151
Max Magnitude0
ClinVar
Risk rs587777151(G;G)
Alt rs587777151(G;G)
Reference rs587777151(C;C)
Significance Pathogenic
Disease Warburg micro syndrome 3
Variation info
Gene RAB18
CLNDBN Warburg micro syndrome 3
Reversed 0
HGVS NC_000010.10:g.27822688C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000087132.3,