Variant (rsID / SNP)

rs6311

rs6311 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HTR2A. Location: chromosome 13, position 47,471,478. Clinical significance in the table: Likely benign.

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Reference-table entries

HTR2ALikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 13:47471478
Cytoband: 13q14.2
HGVS: NM_001378924.1(HTR2A):c.-329+609G>A

Associated conditions / phenotypes

Cocaine-Related Disorders|Obsessive-compulsive disorder, susceptibility to

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.