First published · Last updated
Variant missense en el gen RRAGC associada a malaltia neonatal greu
A journal article reports a missense variant in the RRAGC gene associated with severe neonatal disease. The supplied excerpt names the publisher but provides no further clinical details or scope.
Categories: public-health, science-and-space
Generated scores
Scores are based on the cited reporting and use a 1–10 scale. Read the methodology.
- Confidence
- 6/10
- Geographic reach
- 1/10
- Global importance
- 3/10
- Impact magnitude
- 3/10
- Positivity
- 2/10
- Urgency
- 2/10
Why it matters
The reported gene–disease association is directly relevant to pediatric clinical research and care.

