| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | TH2LCRR, RAD50
+1 more (R1152Q) | Single nucleotide variant (missense variant) | not specified +4 more | GConflicting classifications of pathogenicity |
| | RAD50, TH2-LCR
+1 more (Y1162N) | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +1 more | |
Click to view in NCBI Gene