Gene entry
SAMSN1
SAM domain, SH3 domain and nuclear localization signals 1
- Chromosome
- 21
- Cytoband
- 21q11.2
- Variants (rsID)
- 41
SAMSN1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 21 (region 21q11.2). Its official name is “SAM domain, SH3 domain and nuclear localization signals 1”. The reference table lists 41 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs2822787Not classifiedmissense_variant
- rs62227165Not classifiedmissense_variant
Other listed variants
- rs415503
- rs1556281
- rs1735484
- rs1882911
- rs1980955
- rs2822696
- rs2822710
- rs2822731
- rs2822754
- rs2822759
- rs2822766
- rs2822771
- rs2822783
- rs2822790
- rs2822793
- rs4817229
- rs6516877
- rs9305389
- rs13050730
- rs17003277
- rs17003329
- rs17240640
- rs17274198
- rs28701010
- rs56185490
- rs73161299
- rs73348015
- rs74441562
- rs74780218
- rs74875101
- rs75831487
- rs77416108
- rs77929574
- rs77998753
- rs78101975
- rs79188788
- rs117232602
- rs141116592
- rs150959160
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.
