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Variant (rsID / SNP)

rs200182626

NRXN1

rs200182626 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NRXN1. Location: chromosome 2, position 50,724,578. 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
2:50724578
Cytoband
2p16.3
HGVS
NM_001330078.2(NRXN1):c.2772C>T (p.Tyr924=)
Allele change
Synonymous_Y924Y

Associated conditions / phenotypes

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

Public references

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