[PMID 20615141] Association of the Protein Tyrosine Phosphatase Nonreceptor 22 Haplotypes with Autoimmune Thyroid Disease in the Japanese Population


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

rs2476599

Parent Gene: PTPN22

Importance: 1
Less common allele: A = 32%
More common allele: G = 68%
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