Table 6 Clinical significance of NRG1 variants
From: NRG1 variant effects in patients with Hirschsprung disease
Variant | Clinical Significance | ClinVar ID |
|---|---|---|
c.397G > C (p.V133 L) | Likely benign | RCV000202884.1 |
rs7834206 | 0 | 0 |
rs3735774 | 0 | 0 |
rs75155858 | 0 | 0 |
From: NRG1 variant effects in patients with Hirschsprung disease
Variant | Clinical Significance | ClinVar ID |
|---|---|---|
c.397G > C (p.V133 L) | Likely benign | RCV000202884.1 |
rs7834206 | 0 | 0 |
rs3735774 | 0 | 0 |
rs75155858 | 0 | 0 |