Variant (rsID / SNP)
rs9636391
rs9636391 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NRXN1. Location: chromosome 2, position 50,201,110. Clinical significance in the table: Benign.
Reference-table entries
NRXN1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- missense_variant
- Chromosome / position
- 2:50201110
- HGVS
- NM_001320156.4,c.29T>C,p.Leu10Ser
- Allele change
- Silent
Associated conditions / phenotypes
Pitt-Hopkins-Like Syndrome 2|Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.