Gene entry
TRPM1
transient receptor potential cation channel subfamily M member 1
- Chromosome
- 15
- Cytoband
- 15q13.3
- Variants (rsID)
- 59
TRPM1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 15 (region 15q13.3). Its official name is “transient receptor potential cation channel subfamily M member 1”. The reference table lists 59 variants (rsID) for this gene.
Clinically classified variants
9 reference-table entries with clinical significance.
- rs12913672Benignsingle nucleotide variantCongenital stationary night blindness 1C
- rs17815774Benignsingle nucleotide variantCongenital stationary night blindness 1C
- rs2241493Benignsingle nucleotide variantCongenital stationary night blindness 1C
- rs3784589Benignsingle nucleotide variantCongenital stationary night blindness 1C
- rs61734295Benignsingle nucleotide variantCongenital stationary night blindness 1C
- rs138886378Conflicting interpretationssingle nucleotide variantCongenital stationary night blindness 1C|Retinitis pigmentosa
- rs182549235Conflicting interpretationssingle nucleotide variantCongenital stationary night blindness 1C
- rs191205969Conflicting interpretationssingle nucleotide variantCongenital stationary night blindness 1C|Retinal dystrophy
- rs369742878Conflicting interpretationssingle nucleotide variantCongenital stationary night blindness 1C
Other listed variants
- rs783024
- rs783026
- rs783033
- rs919001
- rs1672408
- rs2959041
- rs3743234
- rs3784590
- rs3784599
- rs3809578
- rs4779814
- rs4779818
- rs4779829
- rs7178742
- rs8025178
- rs8028220
- rs8035624
- rs11070765
- rs11070767
- rs11070796
- rs11635657
- rs11635677
- rs12148567
- rs12911889
- rs16956509
- rs28368894
- rs28425734
- rs28431191
- rs28613966
- rs28805322
- rs35436576
- rs35472543
- rs55856563
- rs59065311
- rs61997150
- rs75034815
- rs75968509
- rs76783849
- rs80231271
- rs117714415
- rs118162154
- rs141540242
- rs180869804
- rs185083296
- rs185642439
- rs188417056
- rs189480480
- rs199596506
- rs200344215
- rs202031791
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.