Gene entry
XG
Xg glycoprotein (Xg blood group)
- Chromosome
- X
- Cytoband
- Xp22.33
- Variants (rsID)
- 42
XG is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xp22.33). Its official name is “Xg glycoprotein (Xg blood group)”. The reference table lists 42 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs3749988Not classifiedmissense_variant
Other listed variants
- rs311121
- rs311122
- rs311123
- rs311150
- rs311171
- rs311173
- rs311183
- rs311191
- rs311196
- rs312232
- rs1419931
- rs1970797
- rs2259750
- rs2535447
- rs4484858
- rs5939117
- rs5939319
- rs5939320
- rs5982868
- rs7062707
- rs35697189
- rs111776585
- rs112398174
- rs112988737
- rs113588749
- rs138618142
- rs140931233
- rs141584360
- rs141741212
- rs142610755
- rs143003919
- rs145903180
- rs146329762
- rs146537918
- rs147858239
- rs150378456
- rs201628009
- rs753335679
- rs865989371
- rs866048049
- rs868112487
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.