| | | 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 | |
| | | 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 | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | MIR10394, MIR125A +806 more | Copy number gain | See cases | |
| | LOC130064933, LOC130064934 +1093 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |