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rs3789608

From SNPedia

Orientationplus
Stabilizedplus
Make rs3789608(C;C)
Make rs3789608(C;T)
Make rs3789608(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position113855166
GeneMIR223, PTPN22
is asnp
is mentioned by
dbSNPrs3789608
ebirs3789608
HLIrs3789608
Exacrs3789608
Varsomers3789608
Maprs3789608
PheGenIrs3789608
hapmaprs3789608
1000 genomesrs3789608
hgdprs3789608
ensemblrs3789608
gopubmedrs3789608
geneviewrs3789608
scholarrs3789608
googlers3789608
pharmgkbrs3789608
gwascentralrs3789608
openSNPrs3789608
23andMers3789608
23andMe allrs3789608
SNP Nexus

SNPshotrs3789608
SNPdbers3789608
MSV3drs3789608
GWAS Ctlgrs3789608
GMAF0.1593
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 19503742OA-icon.png] Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients


[PMID 16175503OA-icon.png] PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis.