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rs17749211

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0
Make rs17749211(C;T)
Make rs17749211(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position118379170
GeneSAMD12
is asnp
is mentioned by
dbSNPrs17749211
ebirs17749211
HLIrs17749211
Exacrs17749211
Varsomers17749211
Maprs17749211
PheGenIrs17749211
hapmaprs17749211
1000 genomesrs17749211
hgdprs17749211
ensemblrs17749211
gopubmedrs17749211
geneviewrs17749211
scholarrs17749211
googlers17749211
pharmgkbrs17749211
gwascentralrs17749211
openSNPrs17749211
23andMers17749211
23andMe allrs17749211
SNP Nexus

SNPshotrs17749211
SNPdbers17749211
MSV3drs17749211
GWAS Ctlgrs17749211
GMAF0.0528
Max Magnitude0
? (C;C) (C;T) (T;T) 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 8E-6
Odds Ratio NR NR