Gene entry
SNTG2
syntrophin gamma 2
- Chromosome
- 2
- Cytoband
- 2p25.3
- Variants (rsID)
- 91
SNTG2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2p25.3). Its official name is “syntrophin gamma 2”. The reference table lists 91 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs4971432Not classifiedsynonymous_variant
Other listed variants
- rs4246558
- rs4305308
- rs4312525
- rs4366936
- rs4453719
- rs4488692
- rs4583504
- rs4586666
- rs4603794
- rs4927600
- rs4927646
- rs4971390
- rs4971411
- rs4971439
- rs6548201
- rs6548285
- rs6717701
- rs7574097
- rs7579418
- rs7579535
- rs7580578
- rs9636494
- rs9677798
- rs9712145
- rs10169243
- rs10178601
- rs10196789
- rs10207582
- rs10210283
- rs10210677
- rs10779977
- rs11127455
- rs11675840
- rs11696059
- rs11894739
- rs11903404
- rs12469446
- rs13007863
- rs13389243
- rs13393336
- rs13406022
- rs28507166
- rs28760535
- rs34404330
- rs34457673
- rs34787379
- rs55734035
- rs56389760
- rs57694894
- rs60132252
- rs61246823
- rs61744692
- rs62107163
- rs62107421
- rs62107423
- rs62107450
- rs67412276
- rs72768852
- rs72770658
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.
