Have questions? Visit https://www.reddit.com/r/SNPedia

rs17758761

From SNPedia

Orientationplus
Stabilizedplus
Make rs17758761(A;A)
Make rs17758761(A;C)
Make rs17758761(C;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position55977164
is asnp
is mentioned by
dbSNPrs17758761
ebirs17758761
HLIrs17758761
Exacrs17758761
Varsomers17758761
Maprs17758761
PheGenIrs17758761
hapmaprs17758761
1000 genomesrs17758761
hgdprs17758761
ensemblrs17758761
gopubmedrs17758761
geneviewrs17758761
scholarrs17758761
googlers17758761
pharmgkbrs17758761
gwascentralrs17758761
openSNPrs17758761
23andMers17758761
23andMe allrs17758761
SNP Nexus

SNPshotrs17758761
SNPdbers17758761
MSV3drs17758761
GWAS Ctlgrs17758761
GMAF0.04591
Max Magnitude
? (A;A) (A;C) (C;C) 28

[PMID 22194214] Replication study of 10 genes showing evidence for association with multiple sclerosis: validation of TMEM39A, IL12B and CBLB [correction of CLBL] genes


[PMID 20007504OA-icon.png] Comprehensive follow-up of the first genome-wide association study of multiple sclerosis identifies KIF21B and TMEM39A as susceptibility loci.