| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Genomic newborn screening: BabyScreen+ v2.0 | NRXN1 | Gene migrated from ENSG00000179915 to ENSG00000179915 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | NRXN1 |
Zornitza Stark gene: NRXN1 was added gene: NRXN1 was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: NRXN1 was set to Unknown Phenotypes for gene: NRXN1 were set to Autism |
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