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Variant (rsID / SNP)

rs143446587

NRXN1

rs143446587 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NRXN1. Location: chromosome 2, position 50,170,891. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

NRXN1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
2:50170891
Cytoband
2p16.3
HGVS
NM_001330078.2(NRXN1):c.4167C>G (p.Pro1389=)
Allele change
Synonymous_P1389P

Associated conditions / phenotypes

Pitt-Hopkins-like syndrome 2|History of neurodevelopmental disorder

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.