| | | Single nucleotide variant (3 prime UTR variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number gain | not specified | |
| | | Single nucleotide variant (synonymous variant) | KLK3-related disorder | |
| | | Single nucleotide variant (synonymous variant) | KLK3-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | KLK3-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | KLK3-related disorder | |
| | | Single nucleotide variant (synonymous variant) | KLK3-related disorder | |
| | | Single nucleotide variant (missense variant) | KLK3-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | KLK3-related disorder | |
| | | Single nucleotide variant (missense variant) | KLK3-related disorder | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | KLK3-related disorder | |
| | | Single nucleotide variant (synonymous variant) | KLK3-related disorder | |
| | | Single nucleotide variant (synonymous variant) | KLK3-related disorder | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | KLK3-related disorder | |
| | | Single nucleotide variant (missense variant) | KLK3-related disorder | |
| | | Single nucleotide variant (intron variant) | KLK3-related disorder | |
| | | Copy number gain | not provided | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not specified | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not specified | |
| | | Copy number gain | not specified | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided | |
| | PPP1R15A, PPP2R1A +308 more | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary angioedema with normal C1Inh | |
| | | Duplication (frameshift variant) | Hereditary angioedema with normal C1Inh | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Copy number gain | not provided | |
| | PGLYRP1, PGLYRP2 +1364 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130065082, LOC130065083 +806 more | Copy number gain | See cases | |
| | LOC130064903, LOC130064904 +1093 more | Copy number gain | See cases | |
| | LOC130064925, LOC130064926 +1081 more | Copy number gain | See cases | |
| | LOC130065034, LOC130065035 +761 more | Copy number gain | See cases | |