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rs9266773

From SNPedia

Orientationplus
Make rs9266773(C;C)
Make rs9266773(C;T)
Make rs9266773(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position31384571
GeneLOC105379647, LOC105379656, LOC105379664
is asnp
is mentioned by
dbSNPrs9266773
ebirs9266773
HLIrs9266773
Exacrs9266773
Varsomers9266773
Maprs9266773
PheGenIrs9266773
hapmaprs9266773
1000 genomesrs9266773
hgdprs9266773
ensemblrs9266773
gopubmedrs9266773
geneviewrs9266773
scholarrs9266773
googlers9266773
pharmgkbrs9266773
gwascentralrs9266773
openSNPrs9266773
23andMers9266773
23andMe allrs9266773
SNP Nexus

SNPshotrs9266773
SNPdbers9266773
MSV3drs9266773
GWAS Ctlgrs9266773
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 27559181] Role of genetic susceptibility variants in predicting clinical course in multiple sclerosis: a cohort study.