Variant (rsID / SNP)

rs6267

rs6267 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COMT. Location: chromosome 22, position 19,950,263. Clinical significance in the table: drug response; risk factor.

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Reference-table entries

COMTDrug response

Clinical significance (as recorded): drug response; risk factor
Variant type: single nucleotide variant
Chromosome / position: 22:19950263
Cytoband: 22q11.21
HGVS: NM_000754.4(COMT):c.214G>T (p.Ala72Ser)
Allele change: Missense_A72S

Associated conditions / phenotypes

Schizophrenia, susceptibility to|Tramadol response

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.