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rs17419032

From SNPedia

Orientationplus
Stabilizedplus
Make rs17419032(C;C)
Make rs17419032(C;T)
Make rs17419032(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position201029403
GeneLOC101929305
is asnp
is mentioned by
dbSNPrs17419032
ebirs17419032
HLIrs17419032
Exacrs17419032
Varsomers17419032
Maprs17419032
PheGenIrs17419032
hapmaprs17419032
1000 genomesrs17419032
hgdprs17419032
ensemblrs17419032
gopubmedrs17419032
geneviewrs17419032
scholarrs17419032
googlers17419032
pharmgkbrs17419032
gwascentralrs17419032
openSNPrs17419032
23andMers17419032
23andMe allrs17419032
SNP Nexus

SNPshotrs17419032
SNPdbers17419032
MSV3drs17419032
GWAS Ctlgrs17419032
GMAF0.1396
Max Magnitude
? (C;C) (C;T) (T;T) 28
OMIM612381
DescINFLAMMATORY BOWEL DISEASE 23; IBD23
Variant
Relatedalso
[PMID 20007504OA-icon.png] Comprehensive follow-up of the first genome-wide association study of multiple sclerosis identifies KIF21B and TMEM39A as susceptibility loci.