Gene entry
RIN2
Ras and Rab interactor 2
- Chromosome
- 20
- Cytoband
- 20p11.23
- Variants (rsID)
- 91
RIN2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 20 (region 20p11.23). Its official name is “Ras and Rab interactor 2”. The reference table lists 91 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs147968123Benignsingle nucleotide variant
- rs181298473Benignsingle nucleotide variantRIN2 syndrome
- rs188147644Benignsingle nucleotide variant
- rs2076584Benignsingle nucleotide variantRIN2 syndrome
- rs41306763Benignsingle nucleotide variant
- rs78648341Benignsingle nucleotide variant
- rs35142632Conflicting interpretationssingle nucleotide variant
Other listed variants
- rs199557
- rs199593
- rs369005
- rs407633
- rs424408
- rs429007
- rs447737
- rs746804
- rs808716
- rs1003426
- rs1535339
- rs1570159
- rs1884770
- rs2025048
- rs2064948
- rs2064949
- rs2328472
- rs2424251
- rs2424253
- rs3748486
- rs4814907
- rs4814911
- rs6035452
- rs6035459
- rs6035462
- rs6035468
- rs6046326
- rs6046334
- rs6046393
- rs6046396
- rs6046415
- rs6046482
- rs6046504
- rs6081741
- rs6106144
- rs6106154
- rs6112599
- rs6112671
- rs6112679
- rs6132247
- rs6136836
- rs6136870
- rs6136880
- rs6136897
- rs8115361
- rs9653635
- rs11696547
- rs11696602
- rs11697905
- rs12481305
- rs13036479
- rs13040206
- rs13040285
- rs13041670
- rs13042178
- rs13043586
- rs13044506
- rs16981318
- rs16981330
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.
