{{Rsnum
|rsid=8042919
|Gene=TRPM7
|Chromosome=15
|position=50586433
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|GMAF=0.07071
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=TRPM7
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 1.6 | 12.5 | 85.9
| HCB | 2.2 | 11.1 | 86.7
| JPT | 4.5 | 36.4 | 59.1
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 5.5 | 94.5
| CHB | 2.2 | 11.1 | 86.7
| CHD | 0.0 | 10.6 | 89.4
| GIH | 1.0 | 24.0 | 75.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 5.9 | 94.1
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=19405049
|Title=TRPM7 is not associated with amyotrophic lateral sclerosis-parkinsonism dementia complex in the Kii peninsula of Japan
}}

{{omim
|id=605692
|desc=TRANSIENT RECEPTOR POTENTIAL CATION CHANNEL, SUBFAMILY M, MEMBER 7;
|rsnum=8042919
}}

{{omim
|id=605692
|rsnum=8042919
|variant=0001
}}

{{ClinVar
|rsid=8042919
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=50878630
|CHROM=15
|GMAF=0.0705
|dbSNPBuildID=116
|SSR=0
|SAO=1
|VP=0x050168000000150517110100
|GENEINFO=TRPM7:54822
|GENE_NAME=TRPM7
|GENE_ID=54822
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.50878630G>A
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;PMC;SLO;VLD;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.9293; 0.07071
|CLNACC=RCV000005076.1
|CLNDBN=Amyotrophic lateral sclerosis-parkinsonism/dementia complex 1, susceptibility to
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=605692.0001
|COMMON=1
|Disease=Amyotrophic lateral sclerosis-parkinsonism/dementia complex 1
}}

{{PMID Auto
|PMID=19149903
|Title=Common genetic variants of the ion channel transient receptor potential membrane melastatin 6 and 7 (TRPM6 and TRPM7), magnesium intake, and risk of type 2 diabetes in women.
|OA=1
}}

{{PMID Auto
|PMID=19268276
|Title=Genome-wide association study of smoking initiation and current smoking.
|OA=1
}}

{{GET Evidence
|gene=TRPM7
|aa_change=Thr1482Ile
|aa_change_short=T1482I
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs8042919
|overall_frequency_n=761
|overall_frequency_d=9606
|overall_frequency=0.0792213
|n_genomes=7
|n_genomes_annotated=0
|n_haplomes=8
|n_articles=2
|n_articles_annotated=2
|in_omim=Y
|pph2_score=0.017
|nblosum100=3
|autoscore=2
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}