Gene entry
OBSCN
obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF
- Chromosome
- 1
- Cytoband
- 1q42.13
- Variants (rsID)
- 78
OBSCN is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1q42.13). Its official name is “obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF”. The reference table lists 78 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs62621834Benignsingle nucleotide variant
- rs191837710Conflicting interpretationssingle nucleotide variant
- rs1771487Not classifiedmissense_variant
- rs3795809Not classifiedmissense_variant
- rs512253Not classifiedsynonymous_variant
Other listed variants
- rs429335
- rs435776
- rs1188697
- rs1888681
- rs3738685
- rs3795783
- rs3795785
- rs3795787
- rs3795789
- rs3795800
- rs3795811
- rs4653935
- rs6701173
- rs11578521
- rs11581192
- rs11584418
- rs12023551
- rs12061320
- rs41270183
- rs55704206
- rs56015866
- rs56065114
- rs56087721
- rs56174824
- rs56218706
- rs56249237
- rs56346878
- rs61730827
- rs61730829
- rs61827507
- rs62621832
- rs72762066
- rs74142687
- rs75458225
- rs76666590
- rs78577753
- rs78661188
- rs79902706
- rs80298121
- rs111616349
- rs113202278
- rs113376653
- rs114195142
- rs114775166
- rs116266256
- rs117484136
- rs117491185
- rs118005431
- rs139862166
- rs140996408
- rs141295362
- rs142615706
- rs143021118
- rs143612436
- rs143809856
- rs144372515
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.
