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rs17268364

From SNPedia

Orientationplus
Stabilizedplus
Make rs17268364(A;A)
Make rs17268364(A;G)
Make rs17268364(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position203913095
is asnp
is mentioned by
dbSNPrs17268364
ebirs17268364
HLIrs17268364
Exacrs17268364
Varsomers17268364
Maprs17268364
PheGenIrs17268364
hapmaprs17268364
1000 genomesrs17268364
hgdprs17268364
ensemblrs17268364
gopubmedrs17268364
geneviewrs17268364
scholarrs17268364
googlers17268364
pharmgkbrs17268364
gwascentralrs17268364
openSNPrs17268364
23andMers17268364
23andMe allrs17268364
SNP Nexus

SNPshotrs17268364
SNPdbers17268364
MSV3drs17268364
GWAS Ctlgrs17268364
GMAF0.3609
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 19333938] CTLA4/ICOS gene variants and haplotypes are associated with rheumatoid arthritis and primary biliary cirrhosis in the Canadian population


[PMID 19747393OA-icon.png] Improving power in genetic-association studies via wavelet transformation.


[PMID 19956108OA-icon.png] Analysis of 55 autoimmune disease and type II diabetes loci: further confirmation of chromosomes 4q27, 12q13.2 and 12q24.13 as type I diabetes loci, and support for a new locus, 12q13.3-q14.1.