Gene entry
TRPM6
transient receptor potential cation channel subfamily M member 6
- Chromosome
- 9
- Cytoband
- 9q21.13
- Variants (rsID)
- 38
TRPM6 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9q21.13). Its official name is “transient receptor potential cation channel subfamily M member 6”. The reference table lists 38 variants (rsID) for this gene.
Clinically classified variants
8 reference-table entries with clinical significance.
- rs2274924Benignsingle nucleotide variantIntestinal hypomagnesemia 1
- rs2274925Benignsingle nucleotide variantIntestinal hypomagnesemia 1
- rs3750425Benignsingle nucleotide variantIntestinal hypomagnesemia 1
- rs7859201Benignsingle nucleotide variantIntestinal hypomagnesemia 1
- rs143164660Conflicting interpretationssingle nucleotide variantIntestinal hypomagnesemia 1
- rs56290308Conflicting interpretationssingle nucleotide variantIntestinal hypomagnesemia 1
- rs121912625Pathogenicsingle nucleotide variantIntestinal hypomagnesemia 1
- rs869025214Pathogenicsingle nucleotide variantIntestinal hypomagnesemia 1
Other listed variants
- rs877809
- rs1333343
- rs2254229
- rs4991745
- rs6560408
- rs7045949
- rs11144085
- rs13299138
- rs35804026
- rs58586447
- rs62569673
- rs62569730
- rs66591564
- rs72730940
- rs77826848
- rs77967152
- rs79101189
- rs79289883
- rs79452307
- rs111602408
- rs139586014
- rs142043309
- rs145791687
- rs148912866
- rs149123085
- rs150874152
- rs180963446
- rs182809758
- rs191772517
- rs375390431
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.