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Variants identified in TNFA.
| SNP ID | Location | Minor allele frequency (db SNP*) | Minor allele frequency in patients |
|---|---|---|---|
| rs4645838 ins C | 5′ UTR | NA | 0.02 |
| rs3093662 A/G | Intron 1 | 0.079 | 0.01 |
| rs3093664 A/G | Intron 3 | 0.075 | 0.005 |
| rs4645845 C/T | 3′ UTR | 0.001 | 0.02 |
