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rs2857766

From SNPedia

Orientationplus
Stabilizedplus
Make rs2857766(C;C)
Make rs2857766(C;G)
Make rs2857766(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29666226
GeneMOG
is asnp
is mentioned by
dbSNPrs2857766
ebirs2857766
HLIrs2857766
Exacrs2857766
Varsomers2857766
Maprs2857766
PheGenIrs2857766
hapmaprs2857766
1000 genomesrs2857766
hgdprs2857766
ensemblrs2857766
gopubmedrs2857766
geneviewrs2857766
scholarrs2857766
googlers2857766
pharmgkbrs2857766
gwascentralrs2857766
openSNPrs2857766
23andMers2857766
23andMe allrs2857766
SNP Nexus

SNPshotrs2857766
SNPdbers2857766
MSV3drs2857766
GWAS Ctlgrs2857766
GMAF0.2112
Max Magnitude
? (C;C) (C;G) (G;G) 28

[PMID 21084121] HLA polymorphisms in Italian children with autism spectrum disorders: Results of a family based linkage study


[PMID 17509152OA-icon.png] Variation of the myelin oligodendrocyte glycoprotein gene is not primarily associated with multiple sclerosis in the Sardinian population.


[PMID 17928868] A sequence variation in the MOG gene is involved in multiple sclerosis susceptibility in Italy.


[PMID 19167444] Family-based transmission analysis of HLA genetic markers in Sardinian children with autistic spectrum disorders.


[PMID 20800907] Common variation in the MOG gene influences transcript splicing in humans.


[PMID 23032943OA-icon.png] The association of white matter volume in psychotic disorders with genotypic variation in NRG1, MOG and CNP: a voxel-based analysis in affected individuals and their unaffected relatives


GET Evidence
MOG-V171L
aa_change Val171Leu
aa_change_short V171L
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.181999
summary