Variant (rsID / SNP)

rs6318

rs6318 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HTR2C. Clinical significance in the table: Benign.

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Reference-table entries

HTR2CBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Cytoband: Xq23
HGVS: NM_000868.4(HTR2C):c.68= (p.Ser23=)
Allele change: Missense_C23S

Associated conditions / phenotypes

SEROTONIN 5-HT-2C RECEPTOR POLYMORPHISM

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.