Gene entry
NRXN3
neurexin 3
- Chromosome
- 14
- Cytoband
- 14q24.3-q31.1
- Variants (rsID)
- 436
NRXN3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 14 (region 14q24.3-q31.1). Its official name is “neurexin 3”. The reference table lists 436 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs117696080Uncertain significancesingle nucleotide variantAutism
Other listed variants
- rs31349
- rs31363
- rs31396
- rs31404
- rs31431
- rs31434
- rs31451
- rs177195
- rs177228
- rs177240
- rs178376
- rs178377
- rs184347
- rs213563
- rs214018
- rs214023
- rs215945
- rs221421
- rs221430
- rs221446
- rs221459
- rs221497
- rs404787
- rs446820
- rs741523
- rs760215
- rs766024
- rs918270
- rs919773
- rs929920
- rs985956
- rs986980
- rs988387
- rs994401
- rs1008306
- rs1028256
- rs1030127
- rs1080130
- rs1157322
- rs1509152
- rs1531631
- rs1566675
- rs1882816
- rs1895671
- rs1997557
- rs2063984
- rs2178863
- rs2194617
- rs2197988
- rs2205166
- rs2215838
- rs2223032
- rs2242641
- rs2242644
- rs2270964
- rs2272293
- rs2293824
- rs2293847
- rs2365350
- rs2365676
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.