Conotruncal Heart Defects with Normally Related Great Vessels in 22q.11.2 Deletion Syndrome
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Associated Variants (5)
| RSID | Gene | Evidence |
|---|---|---|
| RS75580157 | — | exploratory |
| RS1193773 | — | exploratory |
| RS7720206 | — | exploratory |
| RS9381793 | — | exploratory |
| RS10133981 | — | exploratory |