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rs4953911

From SNPedia

Orientationplus
Stabilizedplus
Make rs4953911(A;A)
Make rs4953911(A;T)
Make rs4953911(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position134311223
GeneMGAT5
is asnp
is mentioned by
dbSNPrs4953911
ebirs4953911
HLIrs4953911
Exacrs4953911
Varsomers4953911
Maprs4953911
PheGenIrs4953911
hapmaprs4953911
1000 genomesrs4953911
hgdprs4953911
ensemblrs4953911
gopubmedrs4953911
geneviewrs4953911
scholarrs4953911
googlers4953911
pharmgkbrs4953911
gwascentralrs4953911
openSNPrs4953911
23andMers4953911
23andMe allrs4953911
SNP Nexus

SNPshotrs4953911
SNPdbers4953911
MSV3drs4953911
GWAS Ctlgrs4953911
Max Magnitude
? (A;A) (A;T) (T;T) 28
GWAS snp
PMID [PMID 20117844]
Trait Multiple sclerosis (severity)
Title MGAT5 alters the severity of multiple sclerosis.
Risk Allele T
P-val 2E-7
Odds Ratio NR NR