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rs587776875

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAG;AAG) 0 common in clinvar
Make rs587776875(-;-)
Make rs587776875(-;AGA)
Make rs587776875(AGA;AGA)
ReferenceGRCh38 38.1/142
Chromosome10
Position27533752
GeneRAB18
is asnp
is mentioned by
dbSNPrs587776875
ebirs587776875
HLIrs587776875
Exacrs587776875
Varsomers587776875
Maprs587776875
PheGenIrs587776875
hapmaprs587776875
1000 genomesrs587776875
hgdprs587776875
ensemblrs587776875
gopubmedrs587776875
geneviewrs587776875
scholarrs587776875
googlers587776875
pharmgkbrs587776875
gwascentralrs587776875
openSNPrs587776875
23andMers587776875
23andMe allrs587776875
SNP Nexus

SNPshotrs587776875
SNPdbers587776875
MSV3drs587776875
GWAS Ctlgrs587776875
Max Magnitude0
ClinVar
Risk rs587776875(;)
Alt rs587776875(;)
Reference rs587776875(AAG;AAG)
Significance Pathogenic
Disease Warburg micro syndrome 3
Variation info
Gene RAB18
CLNDBN Warburg micro syndrome 3
Reversed 0
HGVS NC_000010.10:g.27822681_27822683delAGA
CLNSRC OMIM Allelic Variant
CLNACC RCV000023173.5,