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rs17090640

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common genotype
Make rs17090640(A;A)
Make rs17090640(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position179746494
is asnp
is mentioned by
dbSNPrs17090640
dbSNP (classic)rs17090640
ClinGenrs17090640
ebirs17090640
HLIrs17090640
Exacrs17090640
Gnomadrs17090640
Varsomers17090640
LitVarrs17090640
Maprs17090640
PheGenIrs17090640
Biobankrs17090640
1000 genomesrs17090640
hgdprs17090640
ensemblrs17090640
geneviewrs17090640
scholarrs17090640
googlers17090640
pharmgkbrs17090640
gwascentralrs17090640
openSNPrs17090640
23andMers17090640
SNPshotrs17090640
SNPdbers17090640
MSV3drs17090640
GWAS Ctlgrs17090640
GMAF0.09688
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 3E-6
Odds Ratio NR NR