{{Rsnum
|rsid=1935349
|Gene=HTR7
|Chromosome=10
|position=92594343
|Orientation=minus
|GMAF=0.2456
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 3.1 | 20.3 | 76.6
| HCB | 2.2 | 37.8 | 60.0
| JPT | 9.1 | 43.2 | 47.7
| YRI | 22.2 | 55.6 | 22.2
| ASW | 0.0 | 0.0 | 0.0
| CHB | 2.2 | 37.8 | 60.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PharmGKB
|RSID=rs1935349
|Name_s=
|Gene_s=HTR7
|Feature=
|Evidence=PubMed ID:17600820
|Annotation=This variant is found to be a risk marker for statin induced myalgia
|Drugs=atorvastatin; pravastatin; simvastatin
|Drug Classes=
|Diseases=Myalgia unspecified
|Curation Level=Curated
|PharmGKB Accession ID=PA161615656
}}

{{PMID Auto
|PMID=16385451
|Title=A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.
|OA=1
}}

{{PMID Auto
|PMID=18330705
|Title=Physiogenomic analysis of localized FMRI brain activity in schizophrenia.
|OA=1
}}

{{GET Evidence
|impact=pharmacogenetic
|qualified_impact=Insufficiently evaluated pharmacogenetic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1935349
|overall_frequency_n=42
|overall_frequency_d=128
|overall_frequency=0.328125
|n_genomes=31
|n_genomes_annotated=0
|n_haplomes=38
|n_articles=1
|n_articles_annotated=0
|in_pharmgkb=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}