Gene entry
NIN
ninein
- Chromosome
- 14
- Cytoband
- 14q22.1
- Variants (rsID)
- 38
NIN is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 14 (region 14q22.1). Its official name is “ninein”. The reference table lists 38 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs12882191Benignsingle nucleotide variantSeckel syndrome 7
- rs61755995Benignsingle nucleotide variant
- rs75544578Benignsingle nucleotide variant
- rs78280523Conflicting interpretationssingle nucleotide variant
- rs143976273Uncertain significancesingle nucleotide variant
Other listed variants
- rs2295846
- rs2984277
- rs3783280
- rs4901059
- rs7143959
- rs7149295
- rs7153720
- rs8010709
- rs9323192
- rs10140023
- rs10148593
- rs12588720
- rs17122945
- rs34281449
- rs72681698
- rs74051903
- rs75974508
- rs78281332
- rs117452336
- rs117948605
- rs142655218
- rs142733791
- rs144609230
- rs144624455
- rs147863467
- rs182667346
- rs184108916
- rs185029649
- rs191873665
- rs193024815
- rs199887033
- rs200345108
- rs201581172
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.