| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC111099027, TMPRSS2 (A28T +1 more) | Single nucleotide variant (missense variant) | TMPRSS2-related condition | |
| | LOC117134604, TMPRSS2 (G8R) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | TMPRSS2, LOC111099027 (P59L +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC111099027, TMPRSS2 (T31A +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TMPRSS2, LOC111099027 (D34E) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC117134604, TMPRSS2 (G8V) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | LOC111099027, TMPRSS2 (T75I +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | TMPRSS2, LOC111099027 (Y82D +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | LOC111099027, TMPRSS2 (H18R +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Microsatellite (frameshift variant) | Malignant tumor of prostate | |
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