Variant (rsID / SNP)

rs117696080

rs117696080 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NRXN3. Location: chromosome 14, position 78,951,205. Clinical significance in the table: Uncertain significance.

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Reference-table entries

NRXN3Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 14:78951205
Cytoband: 14q24.3
HGVS: NM_001330195.2(NRXN3):c.758-160258G>A
Allele change: Silent

Associated conditions / phenotypes

Autism

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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