Variant (rsID / SNP)

rs1360780

rs1360780 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FKBP5. Location: chromosome 6, position 35,607,571. Clinical significance in the table: drug response; risk factor.

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Reference-table entries

FKBP5Drug response

Clinical significance (as recorded): drug response; risk factor
Variant type: single nucleotide variant
Chromosome / position: 6:35607571
Cytoband: 6p21.31
HGVS: NM_004117.4(FKBP5):c.106-2636=
Allele change: Silent

Associated conditions / phenotypes

Antidepressant drug treatment, accelerated response to|Major depressive disorder, increased recurrence of depressive episodes in, 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.