Variant (rsID / SNP)

rs7627615

rs7627615 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HTR3E. Location: chromosome 3, position 183,818,416. The table records no clinical significance for this variant.

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Reference-table entries

HTR3ENot classified

Variant type: missense_variant
Chromosome / position: 3:183818416
HGVS: NM_001256614.1,c.256G>A,p.Ala86Thr
Allele change: Silent

Associated conditions / phenotypes

Schizophrenia|Obsessive-Compulsive Disorder

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.