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rs7789940

From SNPedia

Orientationplus
Stabilizedplus
Make rs7789940(A;A)
Make rs7789940(A;G)
Make rs7789940(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position76321913
is asnp
is mentioned by
dbSNPrs7789940
ebirs7789940
HLIrs7789940
Exacrs7789940
Varsomers7789940
Maprs7789940
PheGenIrs7789940
hapmaprs7789940
1000 genomesrs7789940
hgdprs7789940
ensemblrs7789940
gopubmedrs7789940
geneviewrs7789940
scholarrs7789940
googlers7789940
pharmgkbrs7789940
gwascentralrs7789940
openSNPrs7789940
23andMers7789940
23andMe allrs7789940
SNP Nexus

SNPshotrs7789940
SNPdbers7789940
MSV3drs7789940
GWAS Ctlgrs7789940
GMAF0.3402
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21654844OA-icon.png]
Trait
Title Genome-wide association study of severity in multiple sclerosis.
Risk Allele G
P-val 0.000006
Odds Ratio 1.8700 [NR]