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rs1599971

From SNPedia

Orientationminus
Stabilizedplus
Make rs1599971(C;C)
Make rs1599971(C;T)
Make rs1599971(T;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position113834471
GenePTPN22, RP5-1073O3.2
is asnp
is mentioned by
dbSNPrs1599971
ebirs1599971
HLIrs1599971
Exacrs1599971
Varsomers1599971
Maprs1599971
PheGenIrs1599971
hapmaprs1599971
1000 genomesrs1599971
hgdprs1599971
ensemblrs1599971
gopubmedrs1599971
geneviewrs1599971
scholarrs1599971
googlers1599971
pharmgkbrs1599971
gwascentralrs1599971
openSNPrs1599971
23andMers1599971
23andMe allrs1599971
SNP Nexus

SNPshotrs1599971
SNPdbers1599971
MSV3drs1599971
GWAS Ctlgrs1599971
Merged fromRs2797415
GMAF0.337
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 16175503OA-icon.png] PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis.


[PMID 19180477OA-icon.png] Genetic risk factors for rheumatoid arthritis differ in Caucasian and Korean populations.


[PMID 20615141] Association of the protein tyrosine phosphatase nonreceptor 22 haplotypes with autoimmune thyroid disease in the Japanese population.