Rs669607

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Orientationminus
Geno Mag Summary
(G;T) 0 common in complete genomics
Make rs669607(G;G)
Make rs669607(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position28029953
is asnp
is mentioned by
dbSNPrs669607
Exacrs669607
PheGenIrs669607
nextbiors669607
hapmaprs669607
1000 genomesrs669607
hgdprs669607
ensemblrs669607
gopubmedrs669607
geneviewrs669607
scholarrs669607
googlers669607
pharmgkbrs669607
gwascentralrs669607
openSNPrs669607
23andMers669607
23andMe allrs669607
SNP Nexus

SNPshotrs669607
SNPdbers669607
MSV3drs669607
GMAF0.3889
Max Magnitude0
? (G;G) (G;T) (T;T) 28
23andMe blog multiple sclerosis C 1.15x
GWAS snp
PMID [PMID 21833088OA-icon.png]
Trait
Title Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Risk Allele C
P-val 2E-15
Odds Ratio 1.1300 [1.12-1.15]