| | | Single nucleotide variant (splice donor variant) | Rheumatoid arthritis | |
| | | Single nucleotide variant (missense variant +1 more) | Rheumatoid arthritis | |
| | | Single nucleotide variant (missense variant +1 more) | MHC class II deficiency +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | MHC class II deficiency +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | MHC class II deficiency +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | MHC class II deficiency +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | MHC class II deficiency +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | MHC class II deficiency +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | MHC class II deficiency +1 more | |
| | | Single nucleotide variant (missense variant) | Rheumatoid arthritis | |
| | | Single nucleotide variant (missense variant) | Rheumatoid arthritis | |
| | | Single nucleotide variant (missense variant) | not specified +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | PADI4-related disorder +2 more | |
| | | Single nucleotide variant (synonymous variant) | PADI4-related disorder +2 more | |
| | | Single nucleotide variant (missense variant) | PADI4-related disorder +2 more | |
| | | Single nucleotide variant (missense variant) | PADI4-related disorder +2 more | |
| | | Single nucleotide variant (intron variant) | Rheumatoid arthritis +1 more | |
| | | Single nucleotide variant (synonymous variant) | Rheumatoid arthritis +1 more | |
| | | Single nucleotide variant (intron variant) | Rheumatoid arthritis +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Rheumatoid arthritis +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | MHC class II deficiency +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Rheumatoid arthritis +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | MHC class II deficiency +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | MHC class II deficiency +2 more | |
| | | Single nucleotide variant (intron variant) | MHC class II deficiency +1 more | |
| | | Single nucleotide variant (intron variant) | Rheumatoid arthritis +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant | Rheumatoid arthritis | |
| | | Single nucleotide variant (missense variant +1 more) | MHC class II deficiency +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Rheumatoid arthritis +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +6 more | |
| | | Single nucleotide variant | Rheumatoid arthritis | |
| | | Single nucleotide variant (intron variant) | Rheumatoid arthritis | |
| | | Single nucleotide variant (missense variant +1 more) | Rheumatoid arthritis +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | MHC class II deficiency +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | MHC class II deficiency +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | MHC class II deficiency +1 more | |
| | | Single nucleotide variant (nonsense) | Rheumatoid arthritis | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Rheumatoid arthritis +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Rheumatoid arthritis +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | MHC class II deficiency +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | MHC class II deficiency +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Rheumatoid arthritis +1 more | |
| | | Single nucleotide variant (genic upstream transcript variant) | Rheumatoid arthritis | |
| | AP4B1-AS1, PTPN22 (R620W +2 more) | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (intron variant) | Rheumatoid arthritis | |
| | | Single nucleotide variant (intron variant) | Rheumatoid arthritis | |
| | | Single nucleotide variant (intron variant) | Rheumatoid arthritis | |
| | | Single nucleotide variant (intron variant +1 more) | Systemic lupus erythematosus, susceptibility to, 10 +1 more | |