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rs387906655

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906655(C;G)
Make rs387906655(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29659628
GeneMOG
is asnp
is mentioned by
dbSNPrs387906655
ebirs387906655
HLIrs387906655
Exacrs387906655
Varsomers387906655
Maprs387906655
PheGenIrs387906655
hapmaprs387906655
1000 genomesrs387906655
hgdprs387906655
ensemblrs387906655
gopubmedrs387906655
geneviewrs387906655
scholarrs387906655
googlers387906655
pharmgkbrs387906655
gwascentralrs387906655
openSNPrs387906655
23andMers387906655
23andMe allrs387906655
SNP Nexus

SNPshotrs387906655
SNPdbers387906655
MSV3drs387906655
GWAS Ctlgrs387906655
Max Magnitude0
ClinVar
Risk rs387906655(G;G)
Alt rs387906655(G;G)
Reference rs387906655(C;C)
Significance Pathogenic
Disease Narcolepsy 7
Variation info
Gene MOG
CLNDBN Narcolepsy 7
Reversed 0
HGVS NC_000006.11:g.29627405C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000022667.26,