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rs5978649

From SNPedia

Orientationplus
Stabilizedplus
Make rs5978649(A;A)
Make rs5978649(A;G)
Make rs5978649(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position13596999
GeneEGFL6
is asnp
is mentioned by
dbSNPrs5978649
dbSNP (classic)rs5978649
ClinGenrs5978649
ebirs5978649
HLIrs5978649
Exacrs5978649
Gnomadrs5978649
Varsomers5978649
LitVarrs5978649
Maprs5978649
PheGenIrs5978649
Biobankrs5978649
1000 genomesrs5978649
hgdprs5978649
ensemblrs5978649
geneviewrs5978649
scholarrs5978649
googlers5978649
pharmgkbrs5978649
gwascentralrs5978649
openSNPrs5978649
23andMers5978649
SNPshotrs5978649
SNPdbers5978649
MSV3drs5978649
GWAS Ctlgrs5978649
GMAF0.3676
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 23412934OA-icon.png]
Trait Multiple sclerosis
Title A genome-wide association study of brain lesion distribution in multiple sclerosis.
Risk Allele
P-val 4E-6
Odds Ratio NR NR