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Variant (rsID / SNP)

rs587781101

NRXN1

rs587781101 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NRXN1. Location: chromosome 2, position 50,149,370. 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
2:50149370
Cytoband
2p16.3
HGVS
NM_001330078.2(NRXN1):c.4236C>T (p.Gly1412=)
Allele change
Synonymous_G1412G

Associated conditions / phenotypes

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.