{{Rsnum
|rsid=17815774
|Gene=TRPM1
|Chromosome=15
|position=31042159
|Orientation=plus
|GMAF=0.01148
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=TRPM1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 91.2 | 8.8 | 0.0
| HCB | 98.5 | 1.5 | 0.0
| JPT | 99.1 | 0.9 | 0.0
| YRI | 98.6 | 1.4 | 0.0
| ASW | 96.4 | 3.6 | 0.0
| CHB | 98.5 | 1.5 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 97.3 | 2.7 | 0.0
| MEX | 93.1 | 6.9 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 93.1 | 5.9 | 1.0
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=19721433
|Trait=Treatment response to antipsychotics
|Title=Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics
|RiskAllele=
|Pval=0.000003
|OR=9.00
|ORtxt=[NR] % of variance explained
|OA=1
}}

{{PMID|19878917|OA=1
}} Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans.

{{PMID|19896113|OA=1
}} TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness.

{{GET Evidence
|gene=TRPM1
|aa_change=Val605Met
|aa_change_short=V605M
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs17815774
|overall_frequency_n=281
|overall_frequency_d=10624
|overall_frequency=0.0264495
|n_genomes=3
|n_genomes_annotated=0
|n_haplomes=5
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.005
|nblosum100=0
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}